Article
Genetics of hypophosphatasia.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 May 2017
Mornet E
Abstract excerpt
Hypophosphatasia (HPP) is a rare inherited disorder primarily affecting bone and dental mineralization. Although there is a continuum in the severity of the disease, clinical forms may be arbitrarily distinguished on the basis of age at onset and the presence or absence of bone symptoms: perinatal, infantile, juvenile, adult, prenatal benign, and odontological. Severe forms (perinatal and infantile) are...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
