Hereditary sclerosing poikiloderma

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Hereditary sclerosing poikiloderma
Other names: Hereditary sclerosing poikiloderma, Weary type[1]
PMC3271301 jkms-27-225-g002.png
Hyperpigmented, telangiectatic, and atrophic changes on the skin. a) Trunk. b) both axillae.
SpecialtyDermatology

Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.[2]: 576 

See also

References

  1. 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.
  2. 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