Osteoma cutis in Albright's Hereditary Osteodystrophy / 대한피부과학회지
Korean Journal of Dermatology
;
: 493-495, 2004.
Artículo
en Coreano
| WPRIM
| ID: wpr-159986
ABSTRACT
Albright's hereditary osteodystrophy is an inherited syndrome that encompasses endocrinologic anomaly of pseudohypoparathyroidim or less commonly, pseudo-pseudohypoparathyroidism and various physical stigmata such as mental retardation, short stature, skeletal anomaly of the hands, abnormal dentition, round facies, and osteoma cutis. Primary osteoma cutis in this syndrome presents at birth or in early infancy, preceding most of the other manifestations. This case is a typical presentation with osteoma cutis as the sole initial manifestation. Rather unfamiliar to dermatologists, Albright's hereditary osteodystrophy still deserves to be included in the differentials when an isolated case of osteoma cutis presents in a young child.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Osteoma
/
Seudoseudohipoparatiroidismo
/
Cristianismo
/
Facies
/
Parto
/
Dentición
/
Mano
/
Discapacidad Intelectual
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
2004
Tipo del documento:
Artículo
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