| Literature DB >> 2325096 |
L J Hipkin1, I F Casson, J C Davis.
Abstract
A 20 year old male patient presented with lack of sexual development. On examination he was eunuchoidal and hypogonadal, and olfactory function testing showed he was anosmic. Biochemical investigations proved he was hypogonadotrophic. Kallmann's syndrome was therefore diagnosed. His appearance was very different from his alleged identical twin who had undergone a normal puberty and had normal plasma testosterone and gonadotrophin levels. However, the twin was hyposmic. Genetic fingerprinting confirmed the twins were identical. Why Kallman's syndrome was incompletely expressed in one of them is unexplained. The parents and a normally menstruating sister had normal olfactory function.Entities:
Mesh:
Year: 1990 PMID: 2325096 PMCID: PMC1017005 DOI: 10.1136/jmg.27.3.198
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318