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Honeycomb Atrophy |
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Honeycomb Atrophy A rare autosomal recessive [MIM 209700] symmetric dermatopathy (genodermatosis) characterised by skin atrophy with sharply demarcated ‘pits’, variably accompanied by cardiac defects, mental retardation, neurofibromas. Prognosis Usually slowly progressive; spontaneous regression has been reported. Management Dermabrasion, cryotherapy, ultraviolet light radiation, topical medications, CO2 and 585 nm pulsed dye lasers Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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