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Familial benign hypercalcemia

FHH
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Familial benign hypercalcemia" returned 1 free, full-text review articles. First 1 results:
Benign familial hypocalciuric hypercalcemia.
Last Updated: Dec 06, 2011

To review the pathophysiology, clinical features, diagnosis, and management options for benign familial hypocalciuric hypercalcemia.

Familial benign hypercalcemia--from clinical description to molecular genetics.
Last Updated: Nov 13, 2018

Familial benign hypercalcemia (or familial hypocalciuric hypercalcemia), a syndrome of lifelong hypercalcemia inherited as an autosomal dominant trait, is distinct from the multiple endocrine neoplasia syndromes and other forms of inherited parathyroid disease. Familial benign hypercalcemia ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Familial benign hypercalcemia" returned 1 free, full-text editorial articles. First 1 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Familial benign hypercalcemia" returned 6 free, full-text research articles. First few results:
Different vitamin D substrate-product relationship after oral vitamin D supplementation in familial benign hypercalcemia, primary hyperparathyroidism, and healthy controls.
Last Updated: Oct 18, 2016

In healthy subjects and in patients with primary hyperparathyroidism (PH), the administration of a low dose of 25(OH)D (25 μg/day) increases the serum levels of both 25(OH)D and 1,25(OH)(2)D. It is unknown whether this relationship is present in patients affected by familial benign ...

A case report of familial benign hypocalciuric hypercalcemia: a mutation in the calcium-sensing receptor gene.
Last Updated: Nov 13, 2018

Familial benign hypocalciuric hypercalcemia (FBHH) is an autosomal dominant trait with high penetrance, clinically manifesting a relatively benign, lifelong, persistent hypercalcemia and hypocalciuria without hypercalcemic related complications. The calcium-sensing receptor (CaSR) ...

Functional characterization of calcium-sensing receptor codon 227 mutations presenting as either familial (benign) hypocalciuric hypercalcemia or neonatal hyperparathyroidism.
Last Updated: Nov 21, 2013

Familial benign hypocalciuric hypercalcemia (FBHH), in which calcium homeostasis is disordered, can be distinguished from mild primary hyperparathyroidism by the finding of a heterozygous loss-of-function mutation in the calcium-sensing receptor (CaSR). Here, we report a Polish kindred ...

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