Ankyloblepharon filiforme adnatum is a rare congenital anomaly. We report a case of
ankyloblepharon filiforme adnatum in a newborn Caucasian male whose paediatric …

Ankyloblepharon filiforme adnatum (AFA) is a rare congenital anomaly characterized by
partial or complete adhesion of upper and lower eyelids, usually seen as an isolated finding …

Ankyloblepharon Filiforme Adnatum is a rare congenital anomaly wherein the lid margins
are connected by fine bands of extensile tissue which reduce the palpebral fissure by …

Introduction: Ankyloblepharon filiforme adnatum associated with Hay–Wells syndrome is a
rare congenital disease caused by mutations in TP63 gene on the 3q27 chromosome. Here …

Congenital fusion of jaw and its association with ankyloblepharon filiforme adnatum is
reported but is a quite rare congenital benign anomaly. It may be unilateral or bilateral and …

A síndrome de Hay-Wells é uma forma rara de displasia ectodérmica, descrita inicialmente
em 1976 por Hay e Wells, de caráter autossômico dominante com expressão variável …

O anquilobléfaro filiforme congénito (AFC) é uma condição rara caracterizada por uma
fusão palpebral que pode ser parcial ou completa, com risco de ambliopia de privação. Um …

Ankyloblepharon filiforme adnatum (AFA) is a rare congenital anomaly consisting of partial
or complete adhesion of the upper and lower eyelids, and it can be an isolated finding, or …

A1660 g, male infant was born at 32 weeks gestation to a 34-year-old gravida 2 para 1
mother. Pregnancy was complicated by cervical incompetence, and the infant was born via …

Materials and Methods: Newborn male was referred to eye hospital for ophthalmic
examination. It revealed four fine extensible bands of skin in right eye and two bands in left …