Xeroderma: Difference between revisions
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| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"| [[Ablepharon macrostomia syndrome ]], [[ADULT syndrome ]], [[Albright's hereditary osteodystrophy ]], [[Amelo-onycho-hypohidrotic syndrome ]], [[Ampola syndrome ]], [[Barakat syndrome ]], [[Berardinelli-Seip congenital lipodystrophy ]], [Chondrodysplasia punctata ]], [[Chromosome 1q duplication syndrome ]], [[Chromosome 22 trisomy ]], [[Cockayne syndrome ]], [[Dermatoleukodystrophy ]], [[Dermo-odontodysplasia ]], [[Ectodermal dysplasia]], [[Familial hypopituitarism ]], [[Familial hypothyroidism ]], [[Fenton-Wilkinson-Toselano syndrome ]], [[Freire-Maia syndrome ]], [[Grix-Blankenship-Peterson syndrome ]], [[Hereditary Sensory Neuropathy, Type IV ]], [[Hunter-Carpenter-Macdonald syndrome ]], [[Johnston Aarons Schelley syndrome ]], [[Leprechaunism ]], [[Menkes Disease ]], [[Moynahan syndrome ]], [[Multiple system atrophy ]], [[Progeria]], [[Rabson-Mendenhall syndrome ]], [[Schindler disease]], [[Stoll-Alembik-Finck syndrome ]], [[Wiskott-Aldrich Syndrome ]], [[Wrinkly skin syndrome ]] | |bgcolor="Beige"| [[Ablepharon macrostomia syndrome ]], [[ADULT syndrome ]], [[Albright's hereditary osteodystrophy ]], [[Amelo-onycho-hypohidrotic syndrome ]], [[Ampola syndrome ]], [[Barakat syndrome ]], [[Berardinelli-Seip congenital lipodystrophy ]], [[Chondrodysplasia punctata ]], [[Chromosome 1q duplication syndrome ]], [[Chromosome 22 trisomy ]], [[Cockayne syndrome ]], [[Dermatoleukodystrophy ]], [[Dermo-odontodysplasia ]], [[Ectodermal dysplasia]], [[Familial hypopituitarism ]], [[Familial hypothyroidism ]], [[Fenton-Wilkinson-Toselano syndrome ]], [[Freire-Maia syndrome ]], [[Grix-Blankenship-Peterson syndrome ]], [[Hereditary Sensory Neuropathy, Type IV ]], [[Hunter-Carpenter-Macdonald syndrome ]], [[Johnston Aarons Schelley syndrome ]], [[Leprechaunism ]], [[Menkes Disease ]], [[Moynahan syndrome ]], [[Multiple system atrophy ]], [[Progeria]], [[Rabson-Mendenhall syndrome ]], [[Schindler disease]], [[Stoll-Alembik-Finck syndrome ]], [[Wiskott-Aldrich Syndrome ]], [[Wrinkly skin syndrome ]] | ||
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Revision as of 05:39, 12 July 2012
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WikiDoc Resources for Xeroderma |
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Articles |
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Most recent articles on Xeroderma |
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Media |
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Evidence Based Medicine |
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Clinical Trials |
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Ongoing Trials on Xeroderma at Clinical Trials.gov Clinical Trials on Xeroderma at Google
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Guidelines / Policies / Govt |
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US National Guidelines Clearinghouse on Xeroderma
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Books |
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News |
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Commentary |
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Definitions |
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Patient Resources / Community |
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Patient resources on Xeroderma Discussion groups on Xeroderma Directions to Hospitals Treating Xeroderma Risk calculators and risk factors for Xeroderma
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Healthcare Provider Resources |
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Causes & Risk Factors for Xeroderma |
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Continuing Medical Education (CME) |
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International |
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Business |
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Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Aditya Govindavarjhulla, M.B.B.S. [2]
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Overview
Xeroderma (literally "dry skin")is a condition involving the integumentary system, which in most cases can safely be treated with emollients and/or moisturizers. Xeroderma occurs most commonly on the lower legs, arms, the sides of the abdomen and thighs. Symptoms most associated with Xeroderma are scaling (the visible peeling of the outer skin layer), itching and cracks in the skin.
Causes
Xeroderma is a very common condition. It happens more often in the winter where the cold air outside and the hot air inside creates a low relative humidity. This causes the skin to lose moisture and it may crack and peel. Bathing/showering too frequently, especially if one is using harsh soaps, may also contribute to xeroderma. Xeroderma can also be caused by a deficiency of vitamin A, systemic illness, overexposure to sunlight or some medication.