CLINICAL RECOMMENDATION TO THE DIAGNOSTICS AND TREATMENT OF HYPOPHOSPHATASIA IN CHILDREN

• Autors principals: A. A. Baranov (Autor), L. S. Namazova-Baranova (Autor), К. V. Savostianov (Autor), Т. V. Margieva (Autor), E. A. Vishneva (Autor), G. Т. Yakhyaeva (Autor)
• Format: Llibre
• Publicat: Union of pediatricians of Russia, 2017-02-01T00:00:00Z.
• Matèries: article
• Accés en línia: Connect to this object online.

Hypophosphatasia is a rare genetic disorder caused by deficiency of tissue-specific  alkaline phosphatase as a result of mutations in the ALPL gene. Depending on the form and severity of the disease, pathology may spawn in utero, in childhood or in adult age. Given functions of alkaline phosphatase,...