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Indian J Ophthalmol ; 2010 Jul; 58(4): 323-325
Article in English | IMSEAR | ID: sea-136080

ABSTRACT

We report a case of Wildervanck syndrome exhibiting Klippel-Feil anomaly, Duane retraction syndrome and deafness. Since the first case was reported in 1952, there have been more reports describing this triad, either complete or incomplete. Our patient had the complete triad of the syndrome along with cleft palate and short stature. Also, a review of the literature regarding this syndrome is presented here.


Subject(s)
Adolescent , Cleft Palate/complications , Cleft Palate/surgery , Duane Retraction Syndrome/complications , Dwarfism/complications , Eye Movements/physiology , Female , Goldenhar Syndrome/complications , Goldenhar Syndrome/pathology , Humans , Postoperative Complications , Syndrome
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