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

Khaled A. Elfert; David S. Geller; Carol Nelson-Williams; Richard P. Lifton; Hassan Al-Malki; Awais Nauman

doi:10.12659/AJCR.924527

30 September 2020: Articles

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

Unusual clinical course, Rare disease

Khaled A. Elfert ^A* , David S. Geller ^A , Carol Nelson-Williams ^A , Richard P. Lifton ^A , Hassan Al-Malki ^A , Awais Nauman ^A

DOI: 10.12659/AJCR.924527

Am J Case Rep 2020; 21:e924527

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Figure 3. Conservation of the residues amongst paralogs. Figure 3. illustrates that the leucine is highly conserved among most of the potassium channels in this family of proteins.

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

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