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Crandall syndrome : ウィキペディア英語版
Crandall syndrome
Crandall syndrome is a very rare congenital disorder characterised by progressive sensorineural hearing loss, hair loss associated with pili torti, and hypogonadism demonstrated through low levels of luteinising hormone and growth hormone. It is thought to be an autosomal recessive disorder closely related to Björnstad syndrome which presents similarly but without hypogonadism.〔http://www.orpha.net/consor4.01/www/cgi-bin/OC_Exp.php?lng=EN&Expert=202

The condition was first reported by B. F. Crandall in 1973.〔
Crandall, B. F., Samec, L., Sparkes, R. S., Wright, S. W. A familial syndrome of deafness, alopecia, and hypogonadism. J. Pediat. 82: 461–465, 1973. (4698933 )

==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Crandall syndrome」の詳細全文を読む



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