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Up to: Inborn errors of metabolism · Hereditary hypoparathyroidism
Familial hypoparathyroidism
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects.
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Autosomal dominant hypocalcemia 9 trials · 10 incl. sub-types Sub-types →