1. An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.
- Author
-
Moez Gribaa, Mohamed Younes, Yosra Bouyacoub, Wided Korbaa, Ilhem Ben Charfeddine, Mongi Touzi, Labiba Adala, Ons Mamay, Naceur Bergaoui, and Ali Saad
- Subjects
RICKETS ,PHENOTYPES ,PHOSPHATES ,FAMILIAL hypophosphatemia ,OSTEOMALACIA ,OSTEOPOROSIS ,BONE abnormalities ,PATHOLOGICAL physiology ,GENETIC mutation - Abstract
Abstract  Autosomal dominant hypophosphatemic rickets (ADHR) is a rare disease, characterized by isolated renal phosphate wasting, hypophosphatemia, and inappropriately normal 1,25-dihydroxyvitamin D3 (calcitriol) levels. This syndrome involves rickets with bone deformities in childhood and osteomalacia, osteoporosis, articular and para-articular pain, and fatigue in adulthood. It is caused by mutations in a consensus sequence for proteolytic cleavage of the FGF23 protein. Normally, this protein actively regulates phosphate homeostasis. Here we report a Tunisian family in which one parent and three children show clinical and biological features of ADHR. Mutation analysis of the FGF23 gene finds a heterozygous substitution of the C at position 526 by a T (526 C â T), leading to an amino acid replacement of the FGF23 protein (R176W) at position 176. This causative new mutation is located in the consensus sequence for the proteolytic cleavage domain. These results confirm the importance of this site in FGF23 function and its essential role in ADHR physiopathology. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF