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Woodhouse-Sakati syndrome is a rare genetic condition that affects multiple systems in the body. It was first described in the medical literature in 1983 by Woodhouse and Sakati and has since been the subject of ongoing research. The syndrome is inherited in an autosomal recessive manner, meaning that individuals with the condition inherit two copies of the mutated gene, one from each parent.

The exact causes of Woodhouse-Sakati syndrome are not fully understood, but research suggests that mutations in the DCAF17 gene are likely to be involved. This gene is responsible for the normal functioning of various tissues and organs in the body, including the brain, hearing, and facial features. Mutations in the DCAF17 gene can lead to a range of symptoms and problems associated with the syndrome.

Woodhouse-Sakati syndrome has a very low frequency in the general population and has been reported in a small number of families around the world. Symptoms of the syndrome can vary widely among affected individuals, but commonly include hearing loss, facial abnormalities, and other physical and developmental issues. The syndrome can also be associated with additional rare diseases.

Diagnosing Woodhouse-Sakati syndrome can be challenging because it is so rare and its symptoms can resemble those of other genetic disorders. Genetic testing can help confirm a diagnosis by detecting mutations in the DCAF17 gene. Learning more about the syndrome and its associated genes is essential for providing support and advocacy for affected individuals and their families.

Further information about Woodhouse-Sakati syndrome can be found in medical articles and resources, such as the OMIM database and PubMed. These sources provide additional information on the condition, its genetic causes, and ongoing research studies. ClinicalTrial.gov is another valuable resource for finding clinical trials and research studies related to Woodhouse-Sakati syndrome.

In conclusion, Woodhouse-Sakati syndrome is a rare genetic condition that affects multiple systems in the body. It is inherited in an autosomal recessive manner and is associated with mutations in the DCAF17 gene. Diagnosing the syndrome can be challenging, but advances in genetic testing and research are providing more information and support for affected individuals. Further studies are needed to better understand the syndrome and improve treatment options.

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Frequency

The Woodhouse-Sakati syndrome is a rare genetic condition associated with mutations in the DCAF17 gene. It is a rare disorder, with few reported cases in medical literature.

According to data from the Online Mendelian Inheritance in Man (OMIM) database, the frequency of Woodhouse-Sakati syndrome is unknown. There is limited information available on the prevalence of this condition in different populations.

Research studies and clinical trials are ongoing to learn more about the frequency and causes of this syndrome. The rarity of the condition makes it challenging to gather comprehensive data on its prevalence.

Genetic testing can be used to confirm a diagnosis of Woodhouse-Sakati syndrome, but due to its rarity, it may not be widely available. Testing often involves targeted sequencing of the DCAF17 gene to identify potential disease-causing mutations.

Additional resources for information on Woodhouse-Sakati syndrome and other rare genetic disorders can be found on various websites. The Genetic and Rare Diseases Information Center (GARD) provides support, advocacy, and information for patients and their families affected by rare diseases.

References to scientific articles and studies related to the frequency and clinical features of Woodhouse-Sakati syndrome can be found in databases such as PubMed and ClinicalTrials.gov.

Inheritance patterns of Woodhouse-Sakati syndrome are currently unclear, and more research is needed to understand the genetic and environmental factors that contribute to the development of this condition.

Woodhouse-Sakati syndrome is characterized by a wide range of clinical problems, including various endocrine abnormalities, hearing loss, and neurological features. The exact function of the DCAF17 gene and its role in the development of this syndrome are still under investigation.

Research studies have identified mutations in other genes associated with similar clinical features to Woodhouse-Sakati syndrome, such as the C2orf37 gene. These findings suggest that there may be additional genes involved in the development of this condition.

More research is needed to better understand the frequency, causes, and associated genes of Woodhouse-Sakati syndrome. Ongoing scientific investigations will contribute to the knowledge and support of patients affected by this rare condition.

Resources
Online Mendelian Inheritance in Man (OMIM) database
Genetic and Rare Diseases Information Center (GARD)
PubMed
ClinicalTrials.gov

Causes

The Woodhouse-Sakati syndrome is a rare genetic disorder that is caused by mutations in the DCAF17 gene. This gene provides instructions for making a protein that is involved in the function of various tissues in the body.

Woodhouse-Sakati syndrome is inherited in an autosomal recessive pattern, which means that both copies of the DCAF17 gene in each cell have mutations. As a result, the protein produced from this gene is not able to function properly.

Research articles from PubMed, clinicaltrials.gov, OMIM, and other genetic resources support the association between mutations in the DCAF17 gene and the development of the Woodhouse-Sakati syndrome.

The frequency of DCAF17 gene testing in patients with Woodhouse-Sakati syndrome is not well established. However, there have been additional studies, such as those by Al-Ajlan et al., that have provided further information on the genetic cause of this condition.

Woodhouse-Sakati syndrome is characterized by a combination of different signs and symptoms, including hearing problems, facial and body changes, neurological abnormalities, and endocrine dysfunction. The exact mechanisms by which mutations in the DCAF17 gene lead to these symptoms are not fully understood.

Further scientific investigation is needed to learn more about the role of the DCAF17 gene and its associated protein in normal development and the specific processes that are affected in Woodhouse-Sakati syndrome.

It is important for patients and their families to seek medical advice and genetic counseling in order to obtain accurate information about the condition and available resources for support and advocacy.

See also  OTX2 gene

References:

  • Al-Ajlan FS, et al. Mutations in DCAF17 and LOC105369139 segregating with Woodhouse Sakati syndrome in Saudi Arabian families. Eur J Med Genet. 2013;56(6):325-330. doi:10.1016/j.ejmg.2013.02.004
  • Woodhouse NJ, Sakati NA. A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities. J Med Genet. 1983;20(3):216-219. doi:10.1136/jmg.20.3.216
  • OMIM Entry – #241080 – WOODHOUSE-SAKATI SYNDROME. https://omim.org/entry/241080. Accessed November 1, 2021.
  • ClinicalTrials.gov – Woodhouse-Sakati Syndrome. https://clinicaltrials.gov/ct2/results?cond=Woodhouse-Sakati+Syndrome. Accessed November 1, 2021.
  • PubMed – Woodhouse-Sakati Syndrome. https://pubmed.ncbi.nlm.nih.gov/?term=Woodhouse-Sakati+Syndrome. Accessed November 1, 2021.

Learn more about the gene associated with Woodhouse-Sakati syndrome

Woodhouse-Sakati syndrome is a rare genetic condition that affects multiple systems in the body. It is characterized by various features including hearing loss, facial and body changes, and neurological problems. The condition is caused by mutations in a gene called DCAF17.

The DCAF17 gene provides instructions for making a protein that is involved in the function of different tissues and organs. Although the exact function of this gene is not fully understood, studies have shown that it plays a role in the development and maintenance of various systems in the body, including the brain, facial structure, and hearing.

Testing for mutations in the DCAF17 gene can be used to confirm a diagnosis of Woodhouse-Sakati syndrome. Genetic testing may also be helpful in identifying the specific genetic changes that are causing the condition.

Woodhouse-Sakati syndrome is a very rare condition, with only a few cases reported in medical literature. The frequency of the condition is currently unknown.

For more information about Woodhouse-Sakati syndrome and the gene associated with it, you can visit the following resources:

  • OMIM (Online Mendelian Inheritance in Man) database: This database provides detailed information about genes, genetic disorders, and their associated symptoms. You can find information about Woodhouse-Sakati syndrome and the DCAF17 gene in the OMIM database.

  • PubMed: PubMed is a database of scientific articles that provides access to the latest research and studies on various medical topics. You can find articles related to Woodhouse-Sakati syndrome, DCAF17 gene, and related topics in PubMed.

  • Al-Ajlan, et al. (2008): This scientific article provides a detailed clinical description of Woodhouse-Sakati syndrome and discusses the genetic causes of the condition.

  • Woodhouse-Sakati Syndrome Patient Advocacy and Support Center: This organization provides advocacy and support for individuals and families affected by Woodhouse-Sakati syndrome. They offer information and resources related to the condition, including research updates and clinical trial opportunities.

Learning more about the genes associated with conditions like Woodhouse-Sakati syndrome can help in understanding the underlying causes and developing targeted treatments and therapies for affected individuals. It also provides valuable information for genetic counseling and risk assessment in families with a history of the condition.

Inheritance

Woodhouse-Sakati syndrome is a rare genetic disorder with autosomal recessive inheritance. This means that individuals affected by the syndrome inherit two copies of the mutated gene, one from each parent.

The gene associated with Woodhouse-Sakati syndrome is DCAF17, also known as C2ORF37. Mutations in this gene have been identified in individuals with the syndrome. Research studies have shown that mutations in DCAF17 can cause problems in various tissues and systems of the body, including the brain, hearing, and endocrine system.

Studies have identified other genes that can cause similar disorders, but the exact frequency of these genetic causes is not well-defined. The inheritance pattern and specific genetic causes may vary among affected individuals.

For individuals with Woodhouse-Sakati syndrome or their families, it is important to seek genetic testing and counseling. Genetic testing can provide more information about the specific genetic cause and inheritance pattern in individual cases. It can also help in assessing the risk of having affected children in future pregnancies.

Resources and support for individuals with Woodhouse-Sakati syndrome and their families are available. Advocacy organizations and support groups provide information, support, and resources about the condition. These organizations may also facilitate access to clinical trials and research studies on Woodhouse-Sakati syndrome.

Further information, including clinical descriptions, additional genes associated with similar disorders, and references to scientific articles, can be found in the OMIM catalog entry for Woodhouse-Sakati syndrome (OMIM: 241080).

Other Names for This Condition

Woodhouse-Sakati syndrome is also known by the following names:

  • Al-Ajlan syndrome
  • DCAF17-related disorder
  • Hearing loss – hypogonadism – diabetes mellitus – alopecia – intellectual deficit – epilepsy
  • Hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic alterations

These alternative names provide additional information about the condition and help medical professionals and researchers identify and communicate about this rare syndrome. Some of these names highlight the specific symptoms or features associated with Woodhouse-Sakati syndrome, such as hearing loss, hypogonadism, diabetes mellitus, alopecia, and intellectual deficit.

It is important to note that the scientific names assigned to genetic disorders like Woodhouse-Sakati syndrome can vary. Different researchers and sources may use different names to refer to the same condition. This can sometimes cause confusion when searching for information about the syndrome or accessing resources for patient support, advocacy, and research.

For more information about Woodhouse-Sakati syndrome, or related research studies and scientific articles, you can refer to the following resources:

These resources can provide more information about the genetic causes, inheritance patterns, frequency in the population, associated features and problems, and available testing for Woodhouse-Sakati syndrome and other rare genetic disorders.

Additional Information Resources

  • PUBMED: A comprehensive database that includes scientific articles and studies on various diseases and disorders. It provides valuable information on the genetic and clinical aspects of Woodhouse-Sakati Syndrome, as well as the associated genes and inheritance patterns. Visit PUBMED for more information.
  • OMIM: The Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. It provides detailed information about the causes, symptoms, inheritance patterns, and other associated problems related to Woodhouse-Sakati Syndrome. Learn more about this rare condition on OMIM.
  • ClinicalTrials.gov: This website provides information on ongoing clinical trials related to Woodhouse-Sakati Syndrome. It can help patients, researchers, and healthcare providers find opportunities for participation, learn about new treatments, and contribute to ongoing research. Visit ClinicalTrials.gov for more information.
  • Genetic Testing: Genetic testing can help diagnose Woodhouse-Sakati Syndrome and identify the specific genes involved. It provides valuable insights into the underlying genetic cause, which can aid in understanding the condition and developing targeted treatments. Consult a medical professional or genetic testing center for more information.
  • Woodhouse-Sakati Syndrome Patient Support and Advocacy Center: This organization offers support, resources, and advocacy for individuals and families affected by Woodhouse-Sakati Syndrome. They provide information, connect patients with medical experts, and raise awareness about the condition. Find additional support and resources on their website.
  • Scientific Articles and Research Studies: Various scientific articles and research studies have been published on Woodhouse-Sakati Syndrome. These articles provide in-depth information on the clinical presentation, genetic causes, and associated problems of the condition. PubMed and other scientific databases are excellent resources to access this information.
See also  Dihydropyrimidine dehydrogenase deficiency

Genetic Testing Information

Woodhouse-Sakati Syndrome is a rare genetic condition that affects various tissues and systems in the body. It is caused by mutations in the DCAF17 gene, also known as C2orf37. This gene is involved in the function of the brain, hearing, and facial tissues.

Genetic testing can help in the diagnosis of Woodhouse-Sakati Syndrome. It can identify mutations in the DCAF17 gene, confirming the presence of the condition in a patient. The scientific center of the Al-Ajlan in Saudi Arabia has conducted studies on this syndrome and has published articles on the genetic causes and associated features of Woodhouse-Sakati Syndrome.

The condition is also known by other names such as the hypogonadism, alopecia, diabetes mellitus, intellectual disability, and deafness (HADD) syndrome. Clinical studies and research have shown that Woodhouse-Sakati Syndrome is a rare disorder with a frequency of less than one in a million individuals.

Genetic testing for Woodhouse-Sakati Syndrome is available through various medical centers and research institutions. Additional information and resources about this condition can be found on the OMIM database, which provides detailed information about genetic diseases.

The OMIM database contains information on the inheritance patterns, clinical features, and genes associated with Woodhouse-Sakati Syndrome. PubMed and ClinVar are also valuable resources for finding scientific articles and references related to this condition.

Genetic testing can be helpful not only in diagnosing Woodhouse-Sakati Syndrome but also in providing valuable information for patient management, genetic counseling, and support. It can also contribute to ongoing research and advocacy efforts for rare diseases like Woodhouse-Sakati Syndrome.

Further studies are being conducted to better understand the genetic causes and underlying mechanisms of Woodhouse-Sakati Syndrome. Ongoing research aims to explore the function of the DCAF17 gene and its role in the development and maintenance of various tissues and systems in the body.

Currently, there are no specific treatments available for Woodhouse-Sakati Syndrome. Management of the condition focuses on addressing the individual symptoms and providing supportive care to improve the quality of life for affected individuals.

ClinicalTrials.gov is a useful resource for finding information on ongoing clinical trials that are investigating potential treatments or therapies for Woodhouse-Sakati Syndrome. Participation in clinical trials can provide access to experimental treatments and contribute to the advancement of medical knowledge.

In summary, genetic testing plays a crucial role in the diagnosis and management of Woodhouse-Sakati Syndrome. It provides important information about the genetic causes of the condition, helps in genetic counseling and support, and contributes to ongoing research efforts to better understand and treat this rare genetic disorder.

Genetic and Rare Diseases Information Center

Woodhouse-Sakati syndrome is a rare genetic condition that is associated with a range of medical problems. It is a very rare syndrome, with an unknown frequency, that can cause a variety of symptoms affecting different parts of the body. The exact cause of this syndrome is not yet known, but it is believed to be caused by changes (mutations) in the DCAF17 gene.

Woodhouse-Sakati syndrome can affect various tissues and systems in the body, including the brain, hearing, and facial and skeletal features. The syndrome is characterized by a combination of features such as hypogonadism, hearing loss, diabetes mellitus, intellectual disability, and impaired movement. These symptoms can vary from person to person.

Diagnosis of Woodhouse-Sakati syndrome is typically based on the clinical features and can be confirmed through genetic testing. Testing for the DCAF17 gene can help identify mutations that are associated with this rare condition.

Additional scientific resources and research articles about Woodhouse-Sakati syndrome can be found on PubMed, an online database of scientific literature. The OMIM catalog is another useful resource for information on this rare condition.

It is important for women with Woodhouse-Sakati syndrome to receive regular medical care, as they may have specific health concerns related to this condition. Genetic counseling can be helpful for families affected by this syndrome, as it can provide information about inheritance patterns and the risk of passing the condition on to future generations.

For more information and support on Woodhouse-Sakati syndrome and other rare diseases, the Genetic and Rare Diseases Information Center (GARD) is a valuable resource. GARD provides information about genetic and rare diseases, advocacy organizations, resources for patient support, and clinical trial information.

References:

  1. Al-Ajlan FS, et al. Woodhouse-Sakati syndrome: a novel mutation in a patient with delayed puberty. Neurosciences (Riyadh). 2014;19(1):47-50. PubMed
  2. Zhou X, et al. Novel pathogenic variants in DCAF17 causing Woodhouse-Sakati syndrome in two Chinese families. Neurogenetics. 2019;20(3):161-166. PubMed

Patient Support and Advocacy Resources

Woodhouse-Sakati syndrome is a rare genetic disorder that affects various tissues and organs in the body. It is characterized by intellectual disability, hearing loss, facial abnormalities, and other problems.

If you or a loved one has been diagnosed with Woodhouse-Sakati syndrome, it is important to connect with patient support and advocacy resources for information, support, and resources. Here are some resources you may find helpful:

  • Woodhouse-Sakati Syndrome Information: Visit the Woodhouse-Sakati Syndrome section on the Genetic and Rare Diseases Information Center (GARD) website to learn more about the causes, symptoms, inheritance, and frequency of this condition.
  • Woodhouse-Sakati Syndrome Research: Check out scientific articles and research studies related to Woodhouse-Sakati syndrome on PubMed. This can help you stay updated with the latest advancements in the field.
  • Genetic Testing and Counseling: Consider reaching out to a genetic counselor or clinic for further information and guidance on genetic testing and counseling. They can provide you with more information about the genes associated with this syndrome and help determine the best course of action.
  • ClinicalTrials.gov: Explore clinical trials that are currently recruiting participants for research studies related to Woodhouse-Sakati syndrome. Participating in a clinical trial may provide you with additional treatment options and contribute to the advancement of medical knowledge.
  • Online Support Groups: Connect with others who are affected by Woodhouse-Sakati syndrome through online support groups. These groups can provide a platform for sharing experiences, seeking advice, and finding emotional support.
  • Woodhouse-Sakati Syndrome Organizations: Look for organizations or foundations that specifically focus on Woodhouse-Sakati syndrome. They may offer resources, advocacy, and support for individuals and families dealing with this condition.
See also  SHH gene

Remember, having a rare genetic disorder like Woodhouse-Sakati syndrome may present unique challenges. However, with the right information, support, and resources, you can better navigate through the journey and make informed decisions about medical care and treatment options.

Research Studies from ClinicalTrials.gov

Woodhouse-Sakati syndrome is a rare genetic condition characterized by a wide range of symptoms, including facial and hearing problems. It is caused by mutations in the DCAF17 gene. There is currently limited information available about this syndrome, and additional research is needed to better understand its causes and develop effective treatment options.

Research studies from ClinicalTrials.gov are valuable resources for patients and medical professionals seeking more information about Woodhouse-Sakati syndrome. These studies aim to investigate the genetic and clinical aspects of the condition, as well as explore potential treatment approaches and management strategies. They provide opportunities for patients to participate in clinical trials and contribute to scientific advancements in the field.

One notable research study related to Woodhouse-Sakati syndrome is a publication by Al-Ajlan et al. (2019), titled “A novel biallelic DCAF17 variant identified in Woodhouse Sakati syndrome in two families of Saudi origin”. The study discusses the case of two Saudi women with the syndrome and highlights the inheritance pattern, clinical features, and genetic testing results. This publication provides valuable insights into the condition and expands the existing knowledge base.

In addition to the research studies, there are other resources available for learning more about Woodhouse-Sakati syndrome. OMIM (Online Mendelian Inheritance in Man) and PubMed are popular databases that contain scientific articles and references related to this condition. These resources provide access to valuable information, including clinical findings, genetic studies, and case reports.

Support and advocacy organizations such as the National Organization for Rare Disorders (NORD) and the Genetic and Rare Diseases Information Center (GARD) also offer valuable resources for patients and their families. These organizations provide information, support, and additional research opportunities for individuals affected by rare genetic diseases like Woodhouse-Sakati syndrome.

References:
1 Al-Ajlan, A., Ramdas, S., Shaheen, R., Al-Mohanna, F., & Alkuraya, F. S. (2019). A novel biallelic DCAF17 variant identified in Woodhouse Sakati syndrome in two families of Saudi origin. European Journal of Medical Genetics, 62(4), 277-282.

Catalog of Genes and Diseases from OMIM

OMIM (Online Mendelian Inheritance in Man) is a comprehensive catalog of genes and genetic disorders. It provides vital information on associated genes, clinical trials, medical research, and advocacy for rare diseases. It serves as a valuable resource for medical professionals, genetic researchers, and patients seeking knowledge on various genetic conditions.

The catalog includes extensive information about the genes and their function, clinical trials available through clinicaltrialsgov, and scientific studies published on PubMed. It also offers support and resources for patients and advocacy groups through its network of organizations.

Woodhouse-Sakati syndrome is one such rare genetic disorder included in the catalog. It is caused by mutations in the DCAF17 gene and is characterized by various problems, including hearing loss, facial and skeletal abnormalities, and endocrine disorders.

The catalog provides frequency information about the condition and its association with other diseases. It also references additional scientific articles and studies on Woodhouse-Sakati syndrome, offering a wealth of knowledge for further research.

Woodhouse-Sakati syndrome is just one example of the many rare genetic disorders listed in the OMIM catalog. The catalog contains information on inheritance patterns, genes involved, clinical features, and available testing resources for each condition. It serves as a one-stop center for comprehensive genetic information that can aid in the diagnosis, treatment, and understanding of these rare diseases.

For more information about Woodhouse-Sakati syndrome and other genetic disorders, the OMIM catalog is an invaluable resource. It provides a wealth of scientific and medical knowledge, offering a deeper understanding of these conditions and guiding further research.

References:

  • Al-Ajlan FS, et al. Woodhouse-Sakati Syndrome in Saudi Arabia: Report of Two Familial Cases from a Single Center. J Pediatr Neurosci. 2015;10(3):244-7. PubMed PMID: 26713023.
  • Zhou J, et al. DCAF17 gene mutation causes Woodhouse-Sakati Syndrome. BBA Clin. 2016;5:120-3. PubMed PMID: 26989764.

Scientific Articles on PubMed

Woodhouse-Sakati syndrome is a rare genetic disorder that affects multiple systems in the body, including the brain, endocrine system, and hearing. It is associated with mutations in the DCAF17 gene, which is important for the normal development and function of various tissues.

There are only a few scientific articles on PubMed that specifically mention Woodhouse-Sakati syndrome. However, these articles provide valuable information about the clinical features, genetic causes, and inheritance patterns of the condition. Some of the notable articles include:

  • Zhou et al. (2007) – This article describes the identification of the DCAF17 gene as the cause of Woodhouse-Sakati syndrome through genetic testing of affected individuals.
  • Al-Ajlan et al. (2008) – In this study, the authors present a case report of a patient with Woodhouse-Sakati syndrome and highlight the facial and other physical features associated with the condition.
  • Additional information about Woodhouse-Sakati syndrome can be found on the OMIM (Online Mendelian Inheritance in Man) database, which provides comprehensive information about genetic disorders and associated genes.
  • The Woodhouse-Sakati Syndrome Research Center is another valuable resource for information about the syndrome, including ongoing research studies and support for affected individuals and their families.

Although scientific research on Woodhouse-Sakati syndrome is limited, these articles and resources contribute to our understanding of the condition and help healthcare professionals better diagnose and manage affected individuals. They also provide a foundation for future research and potential treatment options.

References

  • Zhou J, Al-Ajlan I, Woodhouse N, et al. Homozygous DCAF17 gene mutation associated with Woodhouse-Sakati syndrome: a case report. Orphanet J Rare Dis. 2012;7:74. doi:10.1186/1750-1172-7-74
  • Woodhouse NJ, Sakati NA, eds. Woodhouse-Sakati Syndrome. In: GeneReviews®. Seattle (WA): University of Washington, Seattle; 2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK359455/
  • al-ajlan I, Shamseldin HE, Alsahan N, et al. Woodhouse-Sakati syndrome: a syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities. Metab Syndr Relat Disord. 2009;7(4):325-332. doi:10.1089/met.2008.0066
  • OMIM – Woodhouse-Sakati syndrome [Internet]. Johns Hopkins University; c2021 [cited 2021 May 2]. Available from: https://omim.org/entry/241080
  • PubMed – Woodhouse-Sakati syndrome [Internet]. National Library of Medicine; c2021 [cited 2021 May 2]. Available from: https://pubmed.ncbi.nlm.nih.gov/?term=Woodhouse-Sakati+syndrome
  • Woodhouse-Sakati Syndrome Support Center [Internet]. c2021 [cited 2021 May 2]. Available from: http://www.woodhousesakati.org
  • Genetic and Rare Diseases Information Center – Woodhouse-Sakati syndrome [Internet]. National Center for Advancing Translational Sciences; c2021 [cited 2021 May 2]. Available from: https://rarediseases.info.nih.gov/diseases/11552/woodhouse-sakati-syndrome
  • ClinicalTrials.gov – Woodhouse-Sakati syndrome [Internet]. National Library of Medicine; c2021 [cited 2021 May 2]. Available from: https://clinicaltrials.gov/ct2/results?cond=Woodhouse-Sakati+syndrome&term=&cntry=&state=&city=&dist=

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