ba0003pp364 | Other diseases of bone and mineral metabolism | ECTS2014
Whyte Michael
, Leung Edward
, Wilcox William
, Liese Johannes
, Reeves Amy
, Melian Agustin
, Odrljin Tatjana
, Zhang Hui
, Hofmann Christine
Background: Hypophosphatasia (HPP) is caused by inactivating mutation(s) in the gene for tissue non-specific alkaline phosphatase. Extracellular accumulation of inorganic pyrophosphate can lead to profound hypomineralization resulting in limb and chest deformity, respiratory complications and vitamin B6-dependent seizures in the severe forms of HPP. The natural history of HPP is poorly understood, but the perinatal and infantile forms are often considered lethal.<p class="...