Síndrome de Klippel-Feil: Reporte de un caso

Ma Guadalupe Treviño-Alanís, Sergio Salazar-Marioni, Héctor Martínez-Menchaca, Gerardo Rivera-Silva

Resultado de la investigaciónrevisión exhaustiva

Resumen

In 1912 Klippel and Feil described this malady. The Klippel-Feil Syndrome is a hereditary autosomal dominant disease with reduced penetrance and variable expression, its incidence is unknown due to rarity and that most patients are asymptomatic. It is characterized by congenital fusion of two or more cervical vertebrae, low hairline, short neck, and limited mobility. This syndrome is associated with systemic and skeletal alterations. This report describes the radiologic images in a patient with Klippel-Feil syndrome.

Idioma originalSpanish
Páginas (desde-hasta)1-3
Número de páginas3
PublicaciónArchivos de Medicina
Volumen7
N.º5
DOI
EstadoPublished - 1 dic 2011

All Science Journal Classification (ASJC) codes

  • Medicina (todo)

Citar esto