A rare variant of ankyloblepharon filiforme adnatum associated with skin hypopigmentation: A case report from South India.

Abstract:

:We report ankyloblepharon filiforme adnatum (AFA) along with associated skin lesions in a 7-day-old child from South India. It could be a variant of the well described ankyloblepharon-ectodermal defects-cleft lip and palate syndrome also called Hay-Wells syndrome wherein AFA, skin lesions, and clefting are characteristic. The ocular features, genetic inheritance, and possible systemic associations, along with the options for management, are discussed. The need for awareness among ophthalmologists of its systemic associations is discussed to ensure that proper multidisciplinary care is offered to the individuals affected by this rare disorder. This article also highlights the unusual hypopigmented skin lesions found in this infant, which has been scantily reported in the literature, as a possible variation in patients of Indian ethnicity.

journal_name

Indian J Ophthalmol

authors

Kuruvilla SE,Simha AR

doi

10.4103/0301-4738.181741

subject

Has Abstract

pub_date

2016-03-01 00:00:00

pages

241-3

issue

3

eissn

0301-4738

issn

1998-3689

pii

IndianJOphthalmol_2016_64_3_241_181741

journal_volume

64

pub_type

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