Chondrodysplasia punctata is a clinically and genetically diverse group of rare diseases, first described by Erich Conradi (1882–1968), that share the features of stippled epiphyses and skeletal changes.Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. .James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
Types Rhizomelic chondrodysplasia punctata , , X-linked recessive chondrodysplasia punctata Conradi–Hünermann syndrome (chondrodysplasia punctata 2, x-linked dominant) Autosomal dominant chondrodysplasia punctata
See also List of cutaneous conditions List of radiographic findings associated with cutaneous conditions
References
External links