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Hypophosphatasia: Phenotypic Variability and Possible Croatian Origin of the c.1402G>A Mutation of TNSALP Gene

By Danijela Petković Ramadža, Feodora Stipoljev, Vladimir Sarnavka, Davor Begović, Kristina Potočki, Ksenija Fumić, Etienne Mornet and Ivo Barić

Abstract

Hypophosphatasia is a metabolic bone disease characterized by bone and teeth hypomineralization due to defective function of tissue-nonspecific alkaline phosphatase (TNSALP). The disorder is caused by various mutations in the TNSALP gene localized on short arm of chromosome 1. Infantile hypophosphatasia is a severe form of the disease inherited as an autosomal recessive trait which presents before age of six months and often has fatal outcome. We report a patient with typical clinical course for infantile hypophosphatasia who was homozygous for the c.1402G>A mutation. The same mutation has been previously associated with a more severe perinatal form also in a Croatian family what indicates a possible common ancestral origin and phenotypic variability potential of c.1402G>A mutation of TNSALP gene

Topics: hypophosphatasia; alkaline phosphatase; phenotypic variability; infantile form; gene mutations
Publisher: Croatian Anthropological Society
Year: 2009
OAI identifier: oai:hrcak.srce.hr:51511

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