Chondrodysplasia punctata
From Infogalactic: the planetary knowledge core
| Chondrodysplasia punctata | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | Q77.3 |
| DiseasesDB | 32527 31410 34567 |
| Patient UK | Chondrodysplasia punctata |
| MeSH | D002806 |
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
Types include:
- Rhizomelic chondrodysplasia punctata 215100, 222765, 600121
- X-linked recessive chondrodysplasia punctata 302950
- Conradi-Hünermann syndrome 302960
- Autosomal dominant chondrodysplasia punctata 118650
See also
References
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- ↑ 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.
