Title
Hypogonadotropic hypogonadism in a female with the Johnson-McMillin syndrome Hypogonadotropic hypogonadism in a female with the Johnson-McMillin syndrome
Author
Faculty/Department
Faculty of Medicine and Health Sciences
Publication type
article
Publication
St. Louis, Mo ,
Subject
Human medicine
Source (journal)
American journal of obstetrics and gynecology. - St. Louis, Mo
Volume/pages
191(2004) :5 , p. 1728-1729
ISSN
0002-9378
ISI
000225337500037
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Abstract
A case of hypogonadotropic hypogonadism associated with the Johnson-McMillin syndrome is presented. This is a rare, autosomal dominant disorder, characterized by variable degrees of alopecia and anosmia, conductive hearing loss, and increased dental caries. Until now hypogonadotropic hypogonadism has only been observed in affected men. Ovulation can be induced with gonadotropins and conception can be obtained, but because prenatal diagnosis is not as yet possible, oocyte donation should be offered as an alternative for procreation.
E-info
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