Klippel-Feil syndrome: a case report and current understanding of molecular genetic background.
J Indian Med Assoc
;
2007 Apr; 105(4): 213-4, 222
Artigo
em Inglês
| IMSEAR
| ID: sea-104745
ABSTRACT
A case of Klippel-Feil syndrome in a 12-year-old boy presentingwith the features of low set posterior hairline, short webbed neck, scoliosis and Sprengel's deformity associated with upper eyelid coloboma and pre-auricular appendages is described. Radiologically there was evidence of maldeveloped cervical and upper thoracic vertebrae associated with elevated scapula. The association of the eyelid defect and pre-auricular appendages has not been documented in the past. The current literatures based on the recent advances in understanding of molecular genetic control over embryonic development of the cervical spines were reviewed.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Humanos
/
Masculino
/
Criança
/
Resultado do Tratamento
/
Síndrome de Klippel-Feil
/
Biologia Molecular
Idioma:
Inglês
Revista:
J Indian Med Assoc
Ano de publicação:
2007
Tipo de documento:
Artigo
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