Case of an unreported genetic variant of salt losing 3-ß-hydroxysteroid dehydrogenase deficiency.

Alkhatib, Einas H; Adams, Stacie D; Miller, Emily R

Alkhatib, Einas H; Adams, Stacie D; Miller, Emily R.

Afiliación

Alkhatib EH; Department of Pediatrics, Michigan State University/Helen DeVos Children's Hospital, Grand Rapids, Michigan, Grand Rapids, MI, USA.
Adams SD; Division of Pediatric Neurosciences, Section of Pediatric Biochemical Genetics, Michigan State University/Helen DeVos Children's Hospital, Grand Rapids, Michigan, Grand Rapids, MI, USA.
Miller ER; Division of Pediatric Endocrinology, Michigan State University/Helen DeVos Children's Hospital, Grand Rapids, Michigan, 100 MI St NE, Grand Rapids, MI, USA.

Oxf Med Case Reports ; 2021(5): omab021, 2021 May.

Article en En | MEDLINE | ID: mdl-34055358

Palabras clave

adrenal; congenital adrenal hyperplasia; endocrinology; genetics; pediatrics

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Oxf Med Case Reports Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google