Hereditary sclerosing poikiloderma

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Hereditary sclerosing poikiloderma
Other names: Hereditary sclerosing poikiloderma, Weary type[1]
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Hyperpigmented, telangiectatic, and atrophic changes on the skin. a) Trunk. b) both axillae.

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

See also


  1. RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Hereditary sclerosing poikiloderma, Weary type". 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