Cleft lip/palate-intestinal malrotation-cardiopathy syndrome

Cleft lip/palate - intestinal malrotation - cardiopathy is a multiple congenital anomaly syndrome described in 5 patients to date, characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects which were lethal in 3 of the 5 patients reported. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs were reported in individual cases. There have been no further descriptions in the literature since 1997.

Also known as: McPherson-Clemens syndrome, McPherson Clemens syndrome, cleft LIP/palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease, cleft lip, cleft palate, characteristic facies, intestinal malrotation, and lethal congenital heart disease

0 clinical trials for this condition and its sub-types, 0 tagged with Cleft lip/palate-intestinal malrotation-cardiopathy syndrome itself.