Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report

Hypophosphatasia (HPP) is an inborn error of metabolism characterized by defective bone mineralization caused by a deficiency in alkaline phosphatase (ALP) activity due to mutations in the tissue-nonspecific ALP (TNALP) gene. The clinical expression of the disease is variable. Six forms of HPP are i...

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Detalles Bibliográficos
Autores principales: Demirbilek, Hüseyin, Alanay, Yasemin, Alikaşifoğlu, Ayfer, Topçu, Meral, Mornet, Etienne, Özön, Alev, Kandemir, Nurgün
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2012
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316461/
https://www.ncbi.nlm.nih.gov/pubmed/22394703
http://dx.doi.org/10.4274/jcrpe.473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316461/
https://www.ncbi.nlm.nih.gov/pubmed/22394703
http://dx.doi.org/10.4274/jcrpe.473

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