41 top medical experts on type 3 Familial benign hypercalcemia across 5 countries and 2 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. type 3 Familial benign hypercalcemia: Familial hypocalciuric hypercalcemia (FHH) type 3 is one of three recognized types of FHH , an inherited condition that causes abnormally high levels of calcium in the blood (hypercalcemia). FHH also causes high levels of parathyroid hormone (PTH) and low levels of calcium in the urine (hypocalciuria). In most cases, FHH does not cause signs or symptoms.However, some people with FHH do report symptoms. Signs and symptoms that may occur in some people with FHH type 3 include high magnesium in addition to calcium, general symptoms of hypercalcemia (such as weakness, fatigue, muscle pain, constipation, depression, confusion, and excessive thirst), lower bone mineral density , behavioral disorders, and learning disabilities.FHH type 3 is caused by a mutation in the AP2S1 gene and inheritance is autosomal dominant .Treatment is generally not necessary in people with no signs or symptoms of FHH. In severe cases however, removal of the parathyroid gland (parathyroidectomy) may be recommended.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Type III Familial Benign Hypercalcemia,  Oklahoma variant Familial benign hypercalcemia,  Type III Familial Benign Hypercalcemia,  Oklahoma type familial benign Hypercalcemia,  type 3 familial benign Hypercalcemia,  Type III Familial Hypocalciuric Hypercalcemia,  type 3 familial Hypocalciuric hypercalcemia


  

        

                    


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