Cargando…

Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

OBJECTIVE: Hypophosphatasia (HPP) is a rare, commonly unrecognized hereditary mineralization defect with a dramatically poor prognosis in severe cases. This study is the first to examine the detailed clinical and laboratory characteristics of patients with HPP and healthy carriers in Turkey. METHODS...

Descripción completa

Detalles Bibliográficos
Autores principales: Sağlam, Halil, Erdöl, Şahin, Dorum, Sevil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596804/
https://www.ncbi.nlm.nih.gov/pubmed/28663156
http://dx.doi.org/10.4274/jcrpe.4549