SUN-389 Consequences of Late Diagnosis of 11β-Hydroxylase Deficiency

Background: Steroid 11β-hydroxylase (CYP11B1) deficiency (11βOHD) is the second most common form of congenital adrenal hyperplasia (CAH). CAH is more likely to be missed in boys, particularly in patients with 11βOHD. Here, we report two boys with 11βOHD who presented late and the consequences of lat...

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Detalhes bibliográficos
Publicado no:J Endocr Soc
Main Authors: Sabinkar, Gayatri, Mamidala, Venkata Ramamohan, Sunanda, Tirupati, Sarathi, Vijaya, Dileep, Kumar
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2019
Assuntos:
Adrenal
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6553013/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-389
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