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Wildervanck syndrome associated with cleft palate and short stature.

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.
AuthorsAnand Kumar, Anupam Sahu, Shashikant Shetty, P Vijayalakshmi
JournalIndian journal of ophthalmology (Indian J Ophthalmol) Vol. 58 Issue 4 Pg. 323-5 ( 2010) ISSN: 1998-3689 [Electronic] India
PMID20534924 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Cleft Palate (complications, surgery)
  • Duane Retraction Syndrome (complications)
  • Dwarfism (complications)
  • Eye Movements (physiology)
  • Female
  • Goldenhar Syndrome (complications, pathology)
  • Humans
  • Postoperative Complications
  • Syndrome

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