A Case of IFAP Syndrome with Severe Atopic Dermatitis

Table 1

Clinical features in IFAP syndrome
Ocular	Photophobia, corneal scars, punctate keratopathy, corneal erosion and neovascularization, and atopic keratoconjunctivitis
Neurological	Global developmental delay, seizures, and mild inner cerebral atrophy
Other	Short stature, dysmorphic features such as frontal bossing, choanal atresia, and large ears. Intestinal anomalies such as omphalocele, Hirschsprung's disease, congenital aganglionic megacolon, stenosis of the small intestine, renal, vertebral, and testicular anomalies, inguinal hernia, cleft hands, and recurrent infections