Periodontal manifestation of hypophosphatasia. A family case report
- 1 November 1994
- journal article
- case report
- Published by Wiley in Journal of Clinical Periodontology
- Vol. 21 (10) , 710-716
- https://doi.org/10.1111/j.1600-051x.1994.tb00791.x
Abstract
Hypophosphatasia is a rare inherited disease, the 1st clinical sign of which is often a premature loss of deciduous teeth. We describe clinical, histological and SEM findings of 2 cases of hypophosphatasia from a single family and discuss the pathological mechanisms with reference to the literature.Keywords
This publication has 17 references indexed in Scilit:
- Hypophosphatasia: dental aspects and mode of inheritanceJournal of Clinical Periodontology, 1993
- Permanent teeth in hypophosphatasia: light and electron microscopic studyJournal of Oral Pathology & Medicine, 1991
- Prepubertal periodontitis: a review of diagnostic criteria, pathogenesis, and differential diagnosisJournal of Periodontal Research, 1990
- Laboratory studies of a family manifesting premature exfoliation of deciduous teethJournal of Clinical Periodontology, 1986
- Studies of a Family Manifesting Premature Exfoliation of Deciduous TeethThe Journal of Periodontology, 1985
- Prepubertal Periodontitis. I. Definition of a Clinical Disease Entity,The Journal of Periodontology, 1983
- HypophosphatasiaBritish Dental Journal, 1983
- Adult hypophosphatasia with chondrocalcinosis and arthropathyThe American Journal of Medicine, 1982
- Childhood hypophosphatasia and the premature loss of teeth: A clinical and laboratory study of seven casesOral Surgery, Oral Medicine, Oral Pathology, 1973
- Hypophosphatasia with premature shedding of teeth and aplasia of cementumOral Surgery, Oral Medicine, Oral Pathology, 1962