[Azoospermia and 45,X/46,XY chromosomal mosaicism: a case report]

Autor:	M, Le Chatton, A, Zaccabri, M, Agopiantz, B, Leheup, G, Weryha, B, Foliguet
Jazyk:	francouzština
Rok vydání:	2013
Předmět:	Adult Gonadal Dysgenesis 46 XY Male Chromosomes Human X Chromosomes Human Y Mosaicism Humans Turner Syndrome Chromosome Disorders Azoospermia
Zdroj:	Gynecologie, obstetriquefertilite. 41(3)
ISSN:	1769-6682
Popis:	Chromosomal abnormalities are common in patients with oligozoospermia or azoospermia. We report the case of a 32-year patient, with male phenotype, and without hormonal or morphological abnormalities, with a severely reduced spermatogenesis. It was revealed a 45,X/46,XY gonadal dysgenesis. We have reviewed the various problems inherent in the discovery of this rare gonadal dysgenesis, including genetic, cancer and fertility risks.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::be9d6fe68afa872bd490b9cfa5f639e5 https://pubmed.ncbi.nlm.nih.gov/23498728 Zobrazit plný text záznamu Full Text from ScienceDirect