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disease > genetic disease > hereditary disease > Rombo syndrome

disease > skin appendages disease > skin disease > Rombo syndrome

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Rombo syndrome

Rombo syndrome is a very rare genetic disorder characterized mainly by atrophoderma vermiculatum of the face, multiple milia, telangiectases, acral erythema, peripheral vasodilation with cyanosis and a propensity to develop basal cell carcinomas. (Wikipedia)

syndrome de Rombo

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URI

http://data.loterre.fr/ark:/67375/VH8-ZWPVBTF0-1

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