Oral manifestations of Albright hereditary osteodystrophy: a case report.


Autoria(s): Gomes, Mônica Fernandes; Camargo, Ana Maria Albernaz; Sampaio, Tatiane Alves; Graziozi, Maria Aparecida O C; Armond, Mônica Costa
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

01/07/2002

Resumo

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.

Formato

161-166

Identificador

http://dx.doi.org/10.1590/S0041-87812002000400006

Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo, v. 57, n. 4, p. 161-166, 2002.

0041-8781

http://hdl.handle.net/11449/66919

10.1590/S0041-87812002000400006

S0041-87812002000400006

2-s2.0-0036653559

2-s2.0-0036653559.pdf

Idioma(s)

eng

Relação

Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo

Direitos

openAccess

Palavras-Chave #adolescent #Albright syndrome #case report #female #human #mouth disease #pseudohypoparathyroidism #radiography #Adolescent #Female #Fibrous Dysplasia, Polyostotic #Humans #Pseudohypoparathyroidism #Stomatognathic Diseases
Tipo

info:eu-repo/semantics/article