Walker-Warburg Syndrome: Congenital Neurodysplasia and Bilateral Retinal Folds

Audina Berrocal, Ingrid U. Scott, Harry W Flynn

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A 2-month-old girl with a history of congenital hydrocephalus presented due to "wandering eyes." Initial eye examination at age 2 months showed response to light and a prominent retinal fold that extended through the macula and made contact with the posterior and inferior temporal lens capsule in each eye. Combined with the patient's neurologic findings, the results of the ocular examination led to the diagnosis of Walker-Warburg syndrome. During 5 years of follow-up, the patient developed progressive cataracts in both eyes but maintained ambulatory vision in the left eye. Walker-Warburg syndrome should be included in the differential diagnosis for pediatric patients with a history of prominent retinal folds.

Original languageEnglish
Pages (from-to)256-258
Number of pages3
JournalOphthalmic Surgery Lasers and Imaging
Volume35
Issue number3
StatePublished - May 1 2004

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Walker-Warburg Syndrome
Hydrocephalus
Neurologic Manifestations
Cataract
Lenses
Capsules
Differential Diagnosis
Pediatrics
Light

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Walker-Warburg Syndrome : Congenital Neurodysplasia and Bilateral Retinal Folds. / Berrocal, Audina; Scott, Ingrid U.; Flynn, Harry W.

In: Ophthalmic Surgery Lasers and Imaging, Vol. 35, No. 3, 01.05.2004, p. 256-258.

Research output: Contribution to journalArticle

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