Gorlin-Goltz syndrome
Pakistan Journal of Medical Sciences. 2010; 26 (1): 235-238
em Inglês
| IMEMR
| ID: emr-93467
ABSTRACT
We report a case of Gorlin-Goltz syndrome in a 21-year-old man. Gorlin-Goltz syndrome [basal cell nevus syndrome] is an infrequent hereditary disease with its prevalence varying from 1 / 57,000 to 1/250,000. It is principally characterized by a wide range of developmental abnormalities. Main clinical manifestations include multiple odontogenic keratocysts of the jaws, facial basal cell carcinomas and skeletal anomalies. The prevalence varies from 1/57,000 to 1/250,000
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Hipoplasia Dérmica Focal
/
Síndrome do Nevo Basocelular
/
Prevalência
Tipo de estudo:
Relato de Casos
/
Estudo de prevalência
Limite:
Adulto
/
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Pak. J. Med. Sci.
Ano de publicação:
2010
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