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Coffin-Lowry syndrome is a condition that affects many parts of the body. The signs and symptoms are usually more severe in males than in females, although the features of this disorder range from very mild to severe in affected women.
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Coffin-Lowry syndrome - Wikipedia, the free encyclopedia
Coffin-Lowry syndrome is a genetic disorder that is X-linked dominant and which causes severe mental problems sometimes associated with abnormalities of growth, cardiac abnormalities, kyphoscoliosis,...
en.wikipedia.org/wiki/Coffin-Lowry_syndrome |
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Welcome to The Coffin-Lowry Syndrome Foundation (CLSF). The purpose of CLSF is to provide a clearinghouse for information on Coffin-Lowry Syndrome (CLS), and to provide families affected by CLS a general forum in which to exchange information, ideas and advice.
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What is Coffin-Lowry syndrome? ... A syndrome is a set of specific medical signs, characteristics and symptoms. Coffin-Lowry syndrome was originally described independently by Dr. Coffin and associates in 1966, and again by Dr. Lowry and associates in 1971. In 1975, Dr. Temtamy showed that the cases represented a...
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Coffin Lowry Syndrome information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS) ... What is Coffin Lowry Syndrome?
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Coffin-Lowry syndrome (CLS) is usually characterized by severe-to-profound mental retardation in males; less severely impaired individuals have been reported. Intellect ranges from normal to profoundly retarded in heterozygous females.
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MIM #303600 · Text · Description · Clinical Features · Diagnosis · Mapping · Molecular Genetics · Pathogenesis ...
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The Coffin-Lowry Syndrome Foundation ... Founded 1991. Serves as a clearinghouse for information on Coffin-Lowry syndrome. Forum for exchanging experiences, advice and information with other CLS families.
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