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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Detalles Bibliográficos
Autores principales: Nermoen, Ingrid, Følling, Ivar, Vegge, Kjetil, Larmo, Arne, Nedrebø, Bjørn Gunnar, Husebye, Eystein Sverre, Løvås, Kristian
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728610/
https://www.ncbi.nlm.nih.gov/pubmed/19724639
http://dx.doi.org/10.1155/2009/916891

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728610/
https://www.ncbi.nlm.nih.gov/pubmed/19724639
http://dx.doi.org/10.1155/2009/916891

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