Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Familial hypocalciuric hypercalcemia other diagnostic studies
Introduction
Overview
Overview
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q.
Other Diagnostic Studies
Other Diagnostic Studies
Other diagnostic studies helpful in the diagnosis of familial hypocalciuric hypercalcemia are:[1][2]
- DNA sequencing test
- Detects the following mutations of CASR gene
- Point mutations
- Insertions
- Rearrangements in the coding sequences
- Detects the following mutations of CASR gene
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: