Casos de síndrome de Klippel-Feil en la población prehispánica de las islas de La Gomera y El Hierro

  1. Matilde Mercedes Arnay de la Rosa
  2. Javier Velasco Vázquez
  3. Carlos Emilio González Reimers
Journal:
Tabona: Revista de Prehistoria y de Arqueología

ISSN: 0213-2818

Year of publication: 2005

Issue: 14

Pages: 205-212

Type: Article

Export: RIS

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CIRC

  • Social Sciences: D

Abstract

Klippel-Feil syndrome is an uncommon alteration (1:40000 births) characterized by short neck, low dorsal hairline, and restricted neck mobility, as a result of the fusion of a variable number of cervical vertebrae. In a previous report we described a case of an individual affected by Klippel-Feil syndrome and two atlas vertebrae with abnormalities compatible with atypical forms of the disease in a survey on 121 prehispanic individuals from the island El Hierro (Canary Islands). We here describe a new case from La Gomera, consisting of two cervical vertebrae partially fused by the vertebral bodies and posterior arch. The presence of 3 cases of this rare entity among a relative small amount of individuals analysed raises the possibility that isolation and consanguinity could have played an important role, perhaps even among the population who colonized both islands.