Tags: Disease.
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.The lesions become visible in late childhood began at ages 7 to 10 years and are most pronounced on the face At that time a pronounced somewhat cyanotic redness of the lips and hands was evident as well as moderate follicular atrophy of the skin on the cheeks.