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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis treated with living-donor kidney transplantation: case report.

CEN case reports - 7 May 2026

Kaba Akari, Kaku Keizo, Shingaki Kodai, Kubo Shinsuke, Hisadome Yu, Noguchi Hiroshi, Nishiyama Kei, Okabe Yasuhiro, Nakamura Masafumi

Abstract excerpt

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare genetic disorder characterized by renal magnesium wasting, hypercalciuria, and progressive renal function decline, often culminating in end-stage renal disease (ESRD). This report presents the case of a successful living-donor kidney transplantation from a mother to her 22-year-old son, who was diagnosed with FHHNC. The patient...

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Identifiers

PMID: 42095997
DOI: 10.1007/s13730-026-01103-8
PMCID: PMC13153341

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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