| Literature DB >> 12244336 |
Mônica Fernandes Gomes1, Ana Maria Albernaz Camargo, Tatiane Alves Sampaio, Maria Aparecida O C Graziozi, Mônica Costa Armond.
Abstract
Albright hereditary osteodystrophy is a hereditary metabolic disorder of dominant autosomal etiology that is commonly characterized by short stature, round face, small metacarpus and metatarsus, mental retardation, osteoporosis, subcutaneous calcification, variable hypocalcemia, and hyperphosphatemia. In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteodystrophy, and we discuss her clinical, radiographic, and laboratory test characteristics together with the oral manifestations, and we correlate them with the characteristics found in the literature. We also discuss the odontological management of treatment of related periodontal disease and planning for corrections of related malocclusions.Entities:
Mesh:
Year: 2002 PMID: 12244336 DOI: 10.1590/s0041-87812002000400006
Source DB: PubMed Journal: Rev Hosp Clin Fac Med Sao Paulo ISSN: 0041-8781