fa·mil·i·al hy·po·par·a·thy·roid·ism
inherited isolated hypoparathyroidism characterized by hypocalcemia, hyperphosphatemia, cataracts, intracerebral calcifications, and tetany; all three mendelian forms (sex-linked, autosomal dominant, and recessive) of inheritance are known [MIM*146200, MIM*241400, and MIM*307700]. The autosomal dominant form is caused by mutation in either the parathyroid hormone gene (PTH) on chromosome 11p or the calcium sensing receptor gene (CASR) on 3q.
Farlex Partner Medical Dictionary © Farlex 2012
fa·mil·i·al hy·po·par·a·thy·roid·ism
(fă-milē-ăl hīpō-pară-thīroyd-izm) Inherited isolated hypoparathyroidism characterized by hypocalcemia, hyperphosphatemia, cataracts, intracerebral calcifications, and tetany.
Medical Dictionary for the Dental Professions © Farlex 2012