Torticollis keloids cryptorchidism renal dysplasia
Other Names: Goeminne syndrome; TKC; TKCR 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.
NIH genetic and rare disease info[edit source]
Torticollis keloids cryptorchidism renal dysplasia is a rare disease.
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