A Case Report Of Basal Cell Nevus Syndrome
Journal of the Korean Association of Oral and Maxillofacial Surgeons
;
: 136-140, 2002.
Artigo
em Coreano
| WPRIM
| ID: wpr-99496
ABSTRACT
Basal cell nevus syndrome is inherited as an autosomal dominant trait with variable expressivity. This syndrome comprises a number of abnormalities such as multiple nevoid basal cell carcinomas of the skin, skeletal abnormalities as bifid rib and fusion of vertebrae, central nervous system abnormalities as mental retardation, eye abnormalities, and multiple odontogenic kerato cysts. In 1960, Gorlin and Goltz first described the features of this disease as constituting a true syndrome; since then, it has been realized that it is much more complex and encompassing than initially thought. This patient has many symtoms of basal cell nevus syndrome. we has known multiple jaw cysts through panorama and facial computed tomography. He has hyperchromatism on basal cell through skin biopsy. In ophthalmologic consult, he has blindness on right. On his past medical history, amputation was done on his toes for polyductalism. - So we report with literature reviews
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Costelas
/
Pele
/
Coluna Vertebral
/
Biópsia
/
Carcinoma Basocelular
/
Dedos do Pé
/
Síndrome do Nevo Basocelular
/
Cistos Maxilomandibulares
/
Cistos Odontogênicos
/
Sistema Nervoso Central
Limite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Association of Oral and Maxillofacial Surgeons
Ano de publicação:
2002
Tipo de documento:
Artigo
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