Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

BACKGROUND: Bartter Syndrome is a rare, genetically heterogeneous, mainly autosomal recessively inherited condition characterized by hypochloremic hypokalemic metabolic alkalosis. Mutations in several genes encoding for ion channels localizing to the renal tubules including SLC12A1, KCNJ1, BSND, CLC...

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Detalles Bibliográficos
Autores principales: Najafi, Maryam, Kordi-Tamandani, Dor Mohammad, Behjati, Farkhondeh, Sadeghi-Bojd, Simin, Bakey, Zeineb, Karimiani, Ehsan Ghayoor, Schüle, Isabel, Azarfar, Anoush, Schmidts, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375149/
https://www.ncbi.nlm.nih.gov/pubmed/30760291
http://dx.doi.org/10.1186/s13023-018-0981-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375149/
https://www.ncbi.nlm.nih.gov/pubmed/30760291
http://dx.doi.org/10.1186/s13023-018-0981-5

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