TY - JOUR
T1 - Klippel-Feil syndrome: Case report
T2 - Reporte de un caso
AU - Treviño Alanís, María Guadalupe
AU - Salazar-Marioni, Sergio
AU - Martínez-Menchaca, Héctor
AU - Rivera-Silva, Gerardo
N1 - Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2011
Y1 - 2011
N2 - 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. © iMedPub.
AB - 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. © iMedPub.
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UR - https://www.mendeley.com/catalogue/489abd43-cd68-3330-a7e4-fdbfe7cdc161/
U2 - 10.3823/081
DO - 10.3823/081
M3 - Article
SN - 1698-9465
VL - 7
SP - 1
EP - 3
JO - Archivos de Medicina
JF - Archivos de Medicina
IS - 5
ER -