| Literature DB >> 18279545 |
Adam Fechner1, Shirley Fong, Peter McGovern.
Abstract
Kallmann syndrome is a genetic disorder with the hallmarks of anosmia and hypogonadotrophic hypogonadism. It has a male preponderance. With the elucidation of the genetic pathways involved, affected females and inheritance patterns are becoming more clearly identified. It is an eminently treatable disorder, but it must first be recognized by the physician. With treatment, favorable reproductive outcomes can be attained in addition to maturation of secondary sex characteristics.Entities:
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Year: 2008 PMID: 18279545 DOI: 10.1097/OGX.0b013e3181641278
Source DB: PubMed Journal: Obstet Gynecol Surv ISSN: 0029-7828 Impact factor: 2.347