Search results for "neurocutaneous syndrome"

showing 4 items of 4 documents

2016

Common birthmarks can be an indicator of underlying genetic disease but are often overlooked. Mongolian blue spots (dermal melanocytosis) are usually localized and transient, but they can be extensive, permanent, and associated with extracutaneous abnormalities. Co-occurrence with vascular birthmarks defines a subtype of phakomatosis pigmentovascularis, a group of syndromes associated with neurovascular, ophthalmological, overgrowth, and malignant complications. Here, we discover that extensive dermal melanocytosis and phakomatosis pigmentovascularis are associated with activating mutations in GNA11 and GNAQ, genes that encode Gα subunits of heterotrimeric G proteins. The mutations were det…

0301 basic medicineMutationMongolian spotPathologymedicine.medical_specialtyNeurocutaneous SyndromesGNA11Cell BiologyDermatologyBiologymedicine.disease_causemedicine.diseasebiology.organism_classificationBiochemistryPhenotype3. Good health030207 dermatology & venereal diseases03 medical and health sciences030104 developmental biology0302 clinical medicinePhakomatosis pigmentovascularismedicineMolecular BiologyZebrafishGNAQJournal of Investigative Dermatology
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Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome

2017

0301 basic medicinemedicine.medical_specialtyNeurocutaneous Syndromesbusiness.industryDermatologyConsanguinity030105 genetics & hereditymedicine.diseaseDermatologyResearch Letters3. Good healthMelanosis03 medical and health sciences030104 developmental biologyCorrespondenceResearch LetterMISMATCH REPAIR DEFICIENCYmedicinebusinessBritish Journal of Dermatology
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Sturge-Weber syndrome: a report of 14 cases

2013

Sturge-Weber-Krabe syndrome (SWS), also known as encephalotrigeminalangiomatosis and named the forthfacomatosis, recall the names of the authors who first describedit in its basic clinical, radiological andanatomopathological aspects. We report here 14 cases of Sturge-Weber disease. In 6 of these, despite what had been previously described in literature, an extension of the angioma has been noted in other parts of the body. The study of these subjects stresses not only the need for a pharmacological/neuropsychomotor intervention, but alsothe need of a psychotherapeutic approach, for the emotional and affective implications thatcould derive from this syndrome. The reported cases are similar …

Sturge-Weber syndrome encephalotrigeminalangiomatosis epilepsy neurocutaneous syndrome.Pediatricsmedicine.medical_specialtylcsh:RC435-571Sturge–Weber syndromelcsh:MedicineCase ReportSturge-Weber syndromeDiseaseAngiomaEpilepsyIntervention (counseling)lcsh:PsychiatrymedicineencephalotrigeminalangiomatosisRecallbusiness.industryNeurological statuslcsh:Rmedicine.diseaseSettore MED/39 - Neuropsichiatria InfantilePsychiatry and Mental healthSturge-Webersyndrome encephalotrigeminalangiomatosis epilepsy neurocutaneous syndromeepilepsyneurocutaneous syndromebusinessMental Illness
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Mosaic activating mutations in GNA11 and GNAQ are associated with phakomatosis pigmentovascularis and extensive dermal melanocytosis

2016

Common birthmarks can be an indicator of underlying genetic disease but are often overlooked. Mongolian blue spots (dermal melanocytosis) are usually localized and transient, but they can be extensive, permanent, and associated with extracutaneous abnormalities. Co-occurrence with vascular birthmarks defines a subtype of phakomatosis pigmentovascularis, a group of syndromes associated with neurovascular, ophthalmological, overgrowth, and malignant complications. Here, we discover that extensive dermal melanocytosis and phakomatosis pigmentovascularis are associated with activating mutations in GNA11 and GNAQ, genes that encode Gα subunits of heterotrimeric G proteins. The mutations were det…

WT wild typeDNA Mutational AnalysisMolecular Sequence Datapostzygotic mutationsMutation MissenseSWS Sturge-Weber syndromeDermatologycesioflammeagermlineBiochemistrySkin DiseasesAnimals Genetically Modifiedg-proteinDNA deoxyribonucleic acidMongolian Spotoculodermal melanocytosis[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyGeneticsAnimalsHumansddc:610Phosphorylationchoroidal melanomaMolecular BiologyAllelesZebrafishdiseaseBase SequenceNeurocutaneous Syndromessturge-weberInfantCell Biologymongolian spotPPV phakomatosis pigmentovascularisGTP-Binding Protein alpha SubunitsHEK293 CellsPhenotypeMutationGTP-Binding Protein alpha Subunits Gq-G11Original Articleuveal melanoma[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologySignal Transduction
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