Torticollis-keloids-cryptorchidism-renal dysplasia syndrome

Torticollis-keloids-cryptorchidism-renal dysplasia syndrome is an extremely rare developmental defect during embryogenesis malformation syndrome characterized by congenital muscular torticollis associated with skin anomalies (such as multiple keloids, pigmented nevi, epithelioma), urogenital malformations (including cryptorchidism and hypospadias) and renal dysplasia (e.g. chronic pyelonephritis, renal atrophy). Additional reported features include varicose veins, intellectual disability and musculoskeletal anomalies.

Also known as: Goeminne TKCR syndrome, Goeminne syndrome, TKCR, Tkc, Tkcr syndrome, torticollis keloids cryptorchidism renal dysplasia, torticollis, keloids, cryptorchidism, and renal dysplasia

0 clinical trials for this condition and its sub-types, 0 tagged with Torticollis-keloids-cryptorchidism-renal dysplasia syndrome itself.