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A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).

A case of Kallmann's syndrome in a male is reported. Besides the classical picture of hypogonadotrophic hypogonadism (demonstrated both by endocrine investigation and a testicular biopsy) with anosmia, a number of other unusual features are present including gynaecomastia, agencies of the anter...

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Опубликовано в: :J Med Genet
Главные авторы: Ventruto, V, Cali, A, Farina, L, Festa, B, Ricciardi, I, Sebastio, L
Формат: Artigo
Язык:Inglês
Опубликовано: BMJ Publishing Group 1976
Предметы:
Online-ссылка:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013357/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1271431/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.13.1.71
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