Klippel-Feil syndrome: Case report: Reporte de un caso

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

Research output: Contribution to journalArticlepeer-review


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.
Original languageEnglish
Pages (from-to)1-3
Number of pages3
JournalArchivos de Medicina
Issue number5
Publication statusPublished - 2011

Bibliographical note

Copyright 2019 Elsevier B.V., All rights reserved.

All Science Journal Classification (ASJC) codes

  • General Medicine


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