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Coffin–Lowry syndrome : ウィキペディア英語版 | Coffin–Lowry syndrome
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, as well as auditory and visual abnormalities. ==History== It was characterized by Grange S. Coffin (b. 1923) in 1966 and Robert Brian Lowry (b. 1932) in 1971. Coffin–Lowry syndrome was independently described by Dr. Coffin and his associates in 1966 and later described by Dr. Lowry and associates in 1971. Dr. Temtamy showed that the cases represented a single syndrome in 1975.
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