Late-Onset Bartter Syndrome Type II Due to a Homozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review

Patient: Male, 31-year-old Final Diagnosis: Bartter syndrome Symptoms: Weakness Medication: — Clinical Procedure: — Specialty: Genetics • Nephrology OBJECTIVE: Unusual clinical course BACKGROUND: Bartter syndrome is a rare genetic disease characterized by hypokalemia, metabolic alkalosis, and hyperr...

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Detalles Bibliográficos
Autores principales: Elfert, Khaled A., Geller, David S., Nelson-Williams, Carol, Lifton, Richard P., Al-Malki, Hassan, Nauman, Awais
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534490/
https://www.ncbi.nlm.nih.gov/pubmed/32997650
http://dx.doi.org/10.12659/AJCR.924527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534490/
https://www.ncbi.nlm.nih.gov/pubmed/32997650
http://dx.doi.org/10.12659/AJCR.924527

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