Two Adults with Adrenal Myelolipoma and 21-Hydroxylase Deficiency

We present incidentally discovered adrenal myelolipomas in two adult males with untreated congenital adrenal hyperplasia (CAH). The patients had simple virilizing form of CAH due to mutations in the CYP21 gene coding for 21-hydroxylase; one was heterozygous for the I172N mutation and the other compo...

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Detalhes bibliográficos
Main Authors: Nermoen, Ingrid, Følling, Ivar, Vegge, Kjetil, Larmo, Arne, Nedrebø, Bjørn Gunnar, Husebye, Eystein Sverre, Løvås, Kristian
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2009
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2728610/
https://ncbi.nlm.nih.gov/pubmed/19724639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2009/916891
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