Camacho-Ramírez RI, Avila-Reyes R, González-Cavazos L, Plascencia-Valadéz V, Trejo-Belmonte R, Yunes-Zárraga JLM, Velázquez-Quintana NI

Language: Spanish
References: 9
Page: 16-20
PDF size: 201.92 Kb.

ABSTRACT

Introduction. Since 1884 Paul Julios Möbius describe a syndrome extremely rare characteristic by palsy facial bilateral, in this time the cause precise of presentation still is unknown.
Case report. New born of 12 old days and infant of 3 old months, both male whit palsy facial congenital bilateral. Others features clinics are: high nasal bridge, strabismus, epicanto, ptosis, micrognathia, high palate, stridor laryngeal, feedings and choking problems and talipes equinovarus. The cariotipes and brainstems auditory evoked potentials are normal.
Discussion. Many theories about of the development have made. The more accepted is the nuclei cerebral atrophy. The autosomal dominant inheritances have been reported and is speculated the Moebius locus is localized in the short arm chromosomal 1 or large arm chromosomal 13.

REFERENCES

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