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Hereditary sclerosing poikiloderma

From Wikipedia, the free encyclopedia

Hereditary sclerosing poikiloderma
Other namesHereditary sclerosing poikiloderma, Weary type[1]
This condition is inherited in an autosomal dominant manner.
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. Retrieved 15 March 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  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


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This page was last edited on 6 May 2024, at 00:48
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