Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature review.

Maryam ZahediReyhane Hizomi AraniMaryam RafatiAtieh AmouzegarFarzad Hadaegh

Published in: BMC endocrine disorders (2021)

We presented a patient with FHH phenotype whose common genetic tests were negative. Further research is needed to ascertain other causes leading to similar manifestations.

Keyphrases

case report
genome wide
early onset
gene expression
dna methylation