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SAT-286 A Previously Undescribed Combination of Aromatase Deficiency and Non-Classical Congenital Adrenal Hyperplasia in an Hispanic Teenage Male

Background: Aromatase deficiency (AD) is a rare autosomal recessive genetic disorder caused by loss of function mutation in CYP19A1 leading to normal androgen but low estrogen levels. As a result men with this condition have increased linear bone growth, osteoporosis, insulin resistance and glucose...

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Detalles Bibliográficos
Autores principales: Gottesman, Bethany, Marinkovic, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552174/
http://dx.doi.org/10.1210/js.2019-SAT-286