Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants

Steroid 21-hydroxylase deficiency is the most common cause of congenital adrenal hyperplasia (CAH), usually due to biallelic variants in CYP21A2. Classical 21-hydroxylase deficiency is characterised by virilisation of the external genitalia in females and hypocortisolism. Hyponatremia and hyperkalem...

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Detalles Bibliográficos
Autores principales: Kontbay, Tuğba, Turan, İhsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388050/
https://www.ncbi.nlm.nih.gov/pubmed/33389921
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388050/
https://www.ncbi.nlm.nih.gov/pubmed/33389921
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0219

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