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单词 Thomson Syndrome
释义

Thomson Syndrome

英语百科

Rothmund–Thomson syndrome

(重定向自Thomson Syndrome)
Rothmund–Thomson syndrome has an autosomal recessive pattern of inheritance.

Rothmund–Thomson syndrome (RTS), also known as poikiloderma atrophicans with cataract or poikiloderma congenitale, is a rare autosomal recessive skin condition originally described by August von Rothmund (1830–1906) in 1868. Matthew Sydney Thomson (1894–1969) published further descriptions in 1936.

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