Congenital hyperreninemic hypoaldosteronism: A case report

Congenital hypoaldosteronism is a rare autosomal recessive or dominant endocrinopathy with variable penetrance, secondary to primary defects in aldosterone synthesis that could lead to hypovolemia, hyponatremia, hyperkalemia, failure to thrive, microcephaly, seizures, neurodevelopmental delay, or he...

Descripción completa

Detalles Bibliográficos
Autores principales: Yupanqui, Maria Elvira, Schrader-Florez, Camila, López-Ramírez, Sofía, Valenzuela-Vallejo, Laura, Perez-Barreto, Andrés, Céspedes Salazar, Camila, Forero Ronderos, Catalina, Durán Ventura, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552448/
https://www.ncbi.nlm.nih.gov/pubmed/37811351
http://dx.doi.org/10.1177/2050313X231201724

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552448/
https://www.ncbi.nlm.nih.gov/pubmed/37811351
http://dx.doi.org/10.1177/2050313X231201724

Ejemplares similares