Gitelman syndrome manifesting in early childhood and leading to delayed puberty: a case report

INTRODUCTION: Gitelman syndrome is an inherited autosomal recessive renal salt-wasting disorder. It presents with variable clinical symptoms including muscle weakness and fatigue, and the diagnosis is based on metabolic alkalosis, hypokalemia, hypomagnesemia and hypocalciuria. It is usually diagnose...

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Detalles Bibliográficos
Autores principales: Raza, Farhan, Sultan, Mubashar, Qamar, Khola, Jawad, Ali, Jawa, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470992/
https://www.ncbi.nlm.nih.gov/pubmed/23031616
http://dx.doi.org/10.1186/1752-1947-6-331

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470992/
https://www.ncbi.nlm.nih.gov/pubmed/23031616
http://dx.doi.org/10.1186/1752-1947-6-331

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