A Case of Osteoma Cutis, a Diagnostic Clue for Albright's Hereditary Osteodystrophy / 대한피부과학회지
Korean Journal of Dermatology
; : 435-438, 2009.
Article
em Ko
| WPRIM
| ID: wpr-54964
Biblioteca responsável:
WPRO
ABSTRACT
Albright's hereditary osteodystrophy (AHO) has a broad spectrum of physical findings, including short stature, flattened nasal bridge, round facies, obesity, skeletal anomalies of the hands with brachydactyly, osteoma cutis, mental retardation, dental defects, cataracts, and calcification in the basal ganglia. It also includes endocrinologic abnormalities such as pseudohypoparathyroidism and pseudopseudohypoparathyroidism. Primary osteoma cutis, which can precede other physical findings of AHO, might be a diagnostic clue for AHO. Therefore, close follow-up and regular laboratory tests should be done to detect the early development of AHO in young children with primary osteoma cutis. Early diagnosis and treatment of AHO can prevent irreversible mental retardation and developmental delay.
Palavras-chave
Texto completo:
1
Base de dados:
WPRIM
Assunto principal:
Osteoma
/
Pseudo-Hipoparatireoidismo
/
Pseudopseudo-Hipoparatireoidismo
/
Dermatopatias Genéticas
/
Gânglios da Base
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Doenças Ósseas Metabólicas
/
Catarata
/
Ossificação Heterotópica
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Fácies
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Diagnóstico Precoce
Tipo de estudo:
Diagnostic_studies
/
Screening_studies
Limite:
Child
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Dermatology
Ano de publicação:
2009
Tipo de documento:
Article