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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Detalles Bibliográficos
Autores principales: Sabinkar, Gayatri, Mamidala, Venkata Ramamohan, Sunanda, Tirupati, Sarathi, Vijaya, Dileep, Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553013/
http://dx.doi.org/10.1210/js.2019-SUN-389