- familial hypophosphatemic osteomalacia
- osteomalacia occurring in familial hypophosphatemic rickets.
Medical dictionary. 2011.
Medical dictionary. 2011.
familial hypophosphatemic rickets — any of several inherited disorders of proximal renal tubular function causing phosphate loss, hypophosphatemia, and skeletal deformities, including rickets and osteomalacia. The group is genetically heterogeneous and clinically variable. See X… … Medical dictionary
hypophosphatemic rickets — any of a group of disorders characterized by rickets associated with hypophosphatemia, resulting from dietary phosphorus deficiency (antacid induced osteomalacia) or due to defects in renal tubular function that may be either hereditary (familial … Medical dictionary
Rickets — A disease of infants and children that disturbs normal bone formation (ossification). Rickets is a failure to mineralize bone. This softens bone (producing osteomalacia) and permits marked bending and distortion of bones. Up through the first… … Medical dictionary
Maurice Pechet — 120px Residence Cambridge, Massachusetts Citizenship American … Wikipedia
Fibroblast growth factor 23 — or FGF23 is gene which is a member of the fibroblast growth factor (FGF) family and encodes a protein which is responsible for phosphate metabolism.FGF family members possess broad mitogenic and cell survival activities and are involved in a… … Wikipedia
Fanconi syndrome — Not to be confused with Fanconi anemia. Fanconi syndrome Classification and external resources ICD 10 E72.0 ICD 9 … Wikipedia