Neonatal form of hypophosphatasia. A case report

Hypophosphatasia is a rare (1/100,000), inherited inborn error of metabolism characterized by low serum and tissue alkaline phosphatase activities resulting in skeletal abnormalities. Four clinical forms are recognized depending on the age of diagnosis. Since treatment is not available and th...

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Bibliographic Details
Main Authors: G Tekinalp, B Gürakan, S Yalçin, M Cağlar, H Ergin
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 1995-10-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/3594