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...

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Detalles Bibliográficos
Autores principales: Sağlam, Halil, Erdöl, Şahin, Dorum, Sevil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2017
Materias:
Original Article
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

Internet

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

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