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Soto's_Syndrome
- National Organization for Rare Disorders - NORD provides a general description of Sotos syndrome, gives the alternate name and provides a list of related organizations.
- NINDS - Sotos Syndrome - The National Institute of Neurological Disorders and Stroke gives a definition of this rare genetic disease, the treatments, prognosis, and research being done.
- Sotos Syndrome Support Association of Canada - SSSAC/ACESS aims to provide education and support to Canadian families of persons with cerebral gigantism. Find resources and photos.
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Sirenomelia
- Madison Foundation - Covers sirenomelia syndrome a congenital birth defect. Gives the signs and symptoms, treatment and prognosis.
- Sirenomelia - Gives a description of the disorder and a link to participate in a study; the ISS - International Sirenomelia Study.
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Stickler_Syndrome
- NORD - Stickler Syndrome - The National Organization for Rare Disorders offers a general description of the disorder. Includes alternative names and a list or related organizations.
- Genetics Home Reference - Stickler Syndrome - Find information about this disorder which is characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems.
- MayoClinic - Find an introduction, the signs and symptoms, causes, risk factors, diagnosing and the complications of Stickler syndrome.
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Tay-Sachs
- NORD - Tay Sachs Disease - Find a list of alternative names, a description and a related organizations. From the National Organization for Rare Disorders.
- NINDS - Tay-Sachs Disease - Find an information page from the National Institute of Neurological Disorders and Stroke. Includes treatments, prognoses, research and organizations.
- Genetics Home Reference - Gives information about the rare disease Tay-Sachs. Includes statistics, the genes related to the disease, and further resources.
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Smith-Magenis_Syndrome
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Smith_Lemli_Opitz_Syndrome
- NORD - Smith Lemli Opitz Syndrome - Contains a general description of SLO syndrome, the alternative names and related organizations. From the National Organization for Rare Disorders.
- eMedicine - Features a clinical reference pertaining to Smith-Lemli-Opitz syndrome, written by Dr. Robert D. Steiner.
- Genetics Home Reference - Contains a definition of Smith-Lemli-Opitz syndrome, a developmental disorder. Includes the genes related to the disease, and further resources.
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