A Case of Prenatally Diagnosed Congenital Adrenal Hyperplasia With Brain Morphometric Differences

We report a case of a fetus with a prenatal diagnosis of classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Although CAH is typically assessed postnatally, this fetal case had multiple prenatal clinical assessments made feasible by an interdisciplinary CAH center. The a...

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Detalles Bibliográficos
Autores principales: Rajagopalan, Vidya, Overholtzer, Lloyd Nate, Kim, William S., Wisnowski, Jessica L., Miller, David A., Geffner, Mitchell E., Kim, Mimi S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344108/
https://www.ncbi.nlm.nih.gov/pubmed/35723282
http://dx.doi.org/10.1177/23247096221105245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344108/
https://www.ncbi.nlm.nih.gov/pubmed/35723282
http://dx.doi.org/10.1177/23247096221105245

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