child·hood hy·po·phos·pha·ta·si·a

a relatively mild autosomal recessive form of hypophosphatasia; it may be allelic with congenital hypophosphatasia.

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References in periodicals archive

For this reason, the disease has been divided into the following clinical sub-groups according to age at presentation: perinatal lethal hypophosphatasia (PLH), prenatal benign hypophosphatasia (PBH), infantile hypophosphatasia, childhood hypophosphatasia, adulthood hypophosphatasia, and odontohypophosphatasia (odonto HPP).

Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

Childhood hypophosphatasia due to a de novo missense mutation in the tissue-nonspecific alkaline phosphatase gene.

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

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