Wildervanck syndrome associated with cleft palate and short stature.

Kumar, Anand; Sahu, Anupam; Shetty, Shashikant; Vijayalakshmi, P

Kumar, Anand; Sahu, Anupam; Shetty, Shashikant; Vijayalakshmi, P.

Indian J Ophthalmol ; 2010 Jul; 58(4): 323-325

Article in English | IMSEAR | ID: sea-136080

ABSTRACT

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

Cervico-oculo-acoustic syndrome; Duane retraction syndrome; Klippel Feil anomaly; Wildervanck syndrome

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Postoperative Complications / Syndrome / Female / Humans / Duane Retraction Syndrome / Adolescent / Cleft Palate / Dwarfism / Eye Movements / Goldenhar Syndrome Language: English Journal: Indian J Ophthalmol Year: 2010 Type: Article

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