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2006, Number 1

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Rev Med Hosp Gen Mex 2006; 69 (1)

Klippel-Feil syndrome in newborn

Islas DLP, Hernández NBA
Full text How to cite this article

Language: Spanish
References: 5
Page: 32-35
PDF size: 95.56 Kb.


Key words:

Newborn, Syndrome Klippel-Feil.

ABSTRACT

It is reported from a male newborn that presents compatible physical characteristics with Syndrome of Klippel-Feil. Defined by a triada characteristic; low establishment of the hair, short neck and limitation of the mobility of the neck. This is a rare congenital illness, of the group of the malformations of the Skull-Cervical union, that consists of the congenital fusion of two or more cervical vertebrae.


REFERENCES

  1. Matsuoka T, Ahlberg P. Neural crest origins of the neck and shoulder. Nature 2005; 436: 347-355.

  2. Austrich E, Téllez JF. Síndrome de Klippel-Feil. Imágenes por tomografía en tercera dimensión. Gac Med Mex 2001; l37: 609-6ll.

  3. Curcio C, Burry G, Isasi W. Síndrome de Klippel-Feil. A propósito de un caso. Rev Neurocir 1999; 2.

  4. Fuentes N, Prince JA. Deformidad de Klippel-Feil con anomalía de Arnold-Chiari tipo 1 y siringomielia. Rev Cub Med Mil 2005; 34.

  5. Asociación Nacional Arnold-Chiari. Síndrome de Klippel-Feil. Medicine 1998; 7: 4.166-4.170




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C?MO CITAR (Vancouver)

Rev Med Hosp Gen Mex. 2006;69