Cholestasis-pigmentary retinopathy-cleft palate syndrome

Orpha code: 1415OMIM code: 301068

Definicja

A rare multiple congenital malformation syndrome, 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.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Hardikar syndrome
Zespół Hardikara
Kod ORPHA
1415
Kod OMIM
301068
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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