Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.

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dc.contributor.authorBinitha, M Pen_US
dc.contributor.authorThomas, Daisyen_US
dc.contributor.authorAsha, L Ken_US
dc.date.accessioned2009-05-28T08:12:37Z
dc.date.available2009-05-28T08:12:37Z
dc.date.issued2006-07-02en_US
dc.description.abstractTuberous sclerosis is an autosomal dominant disease due to mutations in two genetic loci, characterized by hamartoma formation in the skin, nervous system, heart, kidney and other organs. Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved and the palms, soles and mucous membranes are usually spared. We report a case of tuberous sclerosis with dyschromatosis universalis hereditaria, with hyperpigmented and hypopigmented macules affecting the palms, soles and oral mucosa. To our knowledge, this is the first reported case of such an association.en_US
dc.description.affiliationDepartment of Dermatology and Venereology, Medical College, Calicut, Kerala, India. mpbinitha@sify.comen_US
dc.identifier.citationBinitha MP, Thomas D, Asha LK. Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria. Indian Journal of Dermatology, Venereology and Leprology. 2006 Jul-Aug; 72(4): 300-2en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/52271
dc.language.isoengen_US
dc.source.urihttps://www.ijdvl.comen_US
dc.subject.meshAdolescenten_US
dc.subject.meshFemaleen_US
dc.subject.meshFoot Dermatoses --complicationsen_US
dc.subject.meshHand Dermatoses --complicationsen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMouth Mucosa --pathologyen_US
dc.subject.meshPigmentation Disorders --complicationsen_US
dc.subject.meshSkin Diseases, Genetic --complicationsen_US
dc.subject.meshTuberous Sclerosis --complicationsen_US
dc.titleTuberous sclerosis complex associated with dyschromatosis universalis hereditaria.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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