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- Rombo_syndrome abstract "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. In adulthood, whitish-yellow, milia-like papules and telangiectatic vessels developed. The papules were present particularly on the cheeks and forehead, gradually becoming very conspicuous and dominating the clinical picture. Trichoepitheliomas were found in 1 case. In adults, the eyelashes and eyebrows were either missing or irregularly distributed with defective and maldirected growth. Basal cell carcinomas were a frequent complication. The skin atrophy was referred to as vermiculate atrophoderma. Basal cell carcinomas may develop around the age of 35. Histological observations during the early stage include irregularly distributed and atrophic hair follicles, milia, dilated dermal vessels, lack of elastin or elastin in clumps. After light irradiation a tendency to increased repair activity was observed both in epidermis and in the dermal fibroblasts.Histologic sections showed the dermis to be almost devoid of elastin in most areas with clumping of elastic material in other areas. The disorder had been transmitted through at least 4 generations with instances of male-to-male transmission.".
- Rombo_syndrome diseasesdb "33487".
- Rombo_syndrome omim "180730".
- Rombo_syndrome wikiPageID "21401093".
- Rombo_syndrome wikiPageRevisionID "592953117".
- Rombo_syndrome diseasesdb "33487".
- Rombo_syndrome hasPhotoCollection Rombo_syndrome.
- Rombo_syndrome name "Rombo syndrome".
- Rombo_syndrome omim "180730".
- Rombo_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Rombo_syndrome subject Category:Genodermatoses.
- Rombo_syndrome subject Category:Rare_diseases.
- Rombo_syndrome subject Category:Syndromes.
- Rombo_syndrome type Abstraction100002137.
- Rombo_syndrome type Attribute100024264.
- Rombo_syndrome type Cognition100023271.
- Rombo_syndrome type Complex105870365.
- Rombo_syndrome type Concept105835747.
- Rombo_syndrome type Condition113920835.
- Rombo_syndrome type Content105809192.
- Rombo_syndrome type Disease114070360.
- Rombo_syndrome type GeneticDisease114151139.
- Rombo_syndrome type GeneticDisordersWithOMIMButNoGene.
- Rombo_syndrome type Idea105833840.
- Rombo_syndrome type IllHealth114052046.
- Rombo_syndrome type Illness114061805.
- Rombo_syndrome type PathologicalState114051917.
- Rombo_syndrome type PhysicalCondition114034177.
- Rombo_syndrome type PsychologicalFeature100023100.
- Rombo_syndrome type State100024720.
- Rombo_syndrome type Syndrome105870790.
- Rombo_syndrome type Syndromes.
- Rombo_syndrome type Whole105869584.
- Rombo_syndrome type Disease.
- Rombo_syndrome type AilmentCondition.
- Rombo_syndrome type Situation.
- Rombo_syndrome comment "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. ".
- Rombo_syndrome label "Rombo syndrome".
- Rombo_syndrome sameAs m.05f4ml2.
- Rombo_syndrome sameAs Q7362935.
- Rombo_syndrome sameAs Q7362935.
- Rombo_syndrome sameAs Rombo_syndrome.
- Rombo_syndrome wasDerivedFrom Rombo_syndrome?oldid=592953117.
- Rombo_syndrome isPrimaryTopicOf Rombo_syndrome.
- Rombo_syndrome name "Rombo syndrome".