Hereditary sclerosing poikiloderma
| Hereditary sclerosing poikiloderma | |
|---|---|
| Other names: Hereditary sclerosing poikiloderma, Weary type[1] | |
 | |
| Hyperpigmented, telangiectatic, and atrophic changes on the skin. a) Trunk. b) both axillae. | |
 | |
| Specialty | Dermatology |
Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.[2]: 576
See also
References
- ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Hereditary sclerosing poikiloderma, Weary type". www.orpha.net. Archived from the original on 16 February 2018. Retrieved 15 March 2019.
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
External links
| Classification |
|---|
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.