Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report

INTRODUCTION: We report the case of a patient with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency who presented with unusual anatomical and biochemical features, namely massively enlarged adrenal glands, adrenogenital rest tissue and an unexpected endocrine profile. The co...

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Detalles Bibliográficos
Autores principales: Ferreira, Florbela, Martins, João Martin, do Vale, Sónia, Esteves, Rui, Nunes, Garção, Carmo, Isabel do
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577455/
https://www.ncbi.nlm.nih.gov/pubmed/23388220
http://dx.doi.org/10.1186/1752-1947-7-39

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577455/
https://www.ncbi.nlm.nih.gov/pubmed/23388220
http://dx.doi.org/10.1186/1752-1947-7-39

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