Chondrodysplasia punctata
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.[1]:500[2]:549
| Chondrodysplasia punctata | |
|---|---|
| Specialty | Medical genetics  |
Types
- Rhizomelic chondrodysplasia punctata 215100, 222765, 600121
- X-linked recessive chondrodysplasia punctata 302950
- Conradi–Hünermann syndrome (chondrodysplasia punctata 2, x-linked dominant) 302960
- Autosomal dominant chondrodysplasia punctata 118650
gollark: It can add somewhat larger numbers!
gollark: https://slatestarcodex.com/2020/06/10/the-obligatory-gpt-3-post/
gollark: Apparently there's a GPT-3 now, and it's basically just a bigger GPT-2 which is somewhat more effective.
gollark: A supervolcano eruption would be *so* 2020.
gollark: Generally you also have special-purpose libraries for various tasks as well as big frameworks for doing a lot of things.
See also
- List of cutaneous conditions
- List of radiographic findings associated with cutaneous conditions
References
- Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
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