Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.[2]: 576
| Hereditary sclerosing poikiloderma | |
|---|---|
| Other names | Hereditary sclerosing poikiloderma, Weary type[1] |
 | |
| This condition is inherited in an autosomal dominant manner. | |
| Specialty | Dermatology |
See also
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edit- ^ 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) - ^ 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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