Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms

Histochemical and direct enzyme analysis of osseous tissue from 23 patients with hypophosphatasia revealed that all clinical forms of this inherited metabolic bone disease are characterized by deficiency of alkaline phosphatase (ALP) activity in bone. The severe infantile form has the most profound...

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Veröffentlicht in:	Medicine (Baltimore) 1984-01, Vol.63 (1), p.12-24
Hauptverfasser:	Fallon, M D, Teitelbaum, S L, Weinstein, R S, Goldfischer, S, Brown, D M, Whyte, M P
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age Factors Alkaline Phosphatase - blood Alkaline Phosphatase - metabolism Biopsy Bone and Bones - enzymology Bone and Bones - pathology Child Child, Preschool Histocytochemistry Humans Hypophosphatasia - enzymology Hypophosphatasia - pathology Infant Minerals - metabolism
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