Hereditary sclerosing poikiloderma

{{Infobox medical condition (new)

| name = Hereditary sclerosing poikiloderma

| synonyms = Hereditary sclerosing poikiloderma, Weary type{{cite web |last1=RESERVED |first1=INSERM US14-- ALL RIGHTS |title=Orphanet: Hereditary sclerosing poikiloderma, Weary type |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=221039 |website=www.orpha.net |accessdate=15 March 2019 |language=en}}

| image = Autosomal dominant - en.svg

| caption = This condition is inherited in an autosomal dominant manner.

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| field = Dermatology

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Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}.{{rp|576}}