Cholestasis-pigmentary retinopathy-cleft palate syndrome

Cholestasis- pigmentary retinopathy- cleft palate is a syndrome of multiple congenital malformations, characterized by an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension etc.) and obstructive renal disease (ectopic ureteric insertion, obstruction, vesicouretral reflux and hydronephrosis). Gastrointestinal tract involvement (malrotation, gastresophageal reflux etc.) and cardiac involvement (coarctation of aorta, pulmonary artery stenosis etc) have also been reported. An overlap with Kabuki syndrome is debated.

Also known as: Hardikar syndrome, HARDIKAR syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Cholestasis-pigmentary retinopathy-cleft palate syndrome itself.