Hutchinson-Gilford progeria syndrome.
Indian J Dermatol Venereol Leprol
; 76(5): 591, 2010.
Article
en En
| MEDLINE
| ID: mdl-20827016
Progeria is a rare genetic disorder characterized by premature aging, involving the skin, bones, heart, and blood vessels. We report a 4-year-old boy who presented with clinical manifestations of progeria. He had characteristic facies, prominent eyes, scalp and leg veins, senile look, loss of scalp hair, eyebrows and eyelashes, stunted growth, and sclerodermatous changes. The present case is reported due to its rarity.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Trastornos de la Pigmentación
/
Esclerodermia Localizada
/
Alopecia
Tipo de estudio:
Etiology_studies
Límite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
Indian J Dermatol Venereol Leprol
Año:
2010
Tipo del documento:
Article
País de afiliación:
India
Pais de publicación:
Estados Unidos