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pro vyhledávání: '"Abir Tahiri"'
Autor:
Achwak Alla, Farel Elilie Mawa Ongoth, Abir Tahiri, Marouan Karrou, Siham Rouf, Houssain Benhaddou, Imane Kamaoui, Kenneth Mcelreavey, Hanane Latrech
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:1215-1221
Objectives We present the first cases of two male brothers with Leydig cell hypoplasia secondary to a novel mutation in the LHCGR gene that has never been described before. Case presentation We report the case of two brothers with Leydig cell hypopla