2022
The genetics and diagnosis of pediatric neurocutaneous disorders: Neurofibromatosis and tuberous sclerosis complex
Tolliver S, Smith Z, Silverberg N. The genetics and diagnosis of pediatric neurocutaneous disorders: Neurofibromatosis and tuberous sclerosis complex. Clinics In Dermatology 2022, 40: 374-382. PMID: 35248688, DOI: 10.1016/j.clindermatol.2022.02.010.Peer-Reviewed Original ResearchConceptsTuberous sclerosis complexMultiple organ systemsNeurocutaneous disorderTarget of rapamycin signaling pathwayClinical featuresGenetic sequencing technologiesSeizure controlLoss of tumor suppressionMitogen-activated protein kinaseCausative genetic mutationsRapamycin signaling pathwayAt-risk family membersSequencing technologiesMammalian target of rapamycin signaling pathwayBenign fibrous growthsCases of NFCafe-au-lait patchesOrgan systemsDisease-specific surveillanceAsh leaf spotsLeaf spotProtein kinaseMosaic conditionSignaling pathwayInstitution of interventions
1991
Disorders of Hypopigmentation in Children
Pinto F, Bolognia J. Disorders of Hypopigmentation in Children. Pediatric Clinics Of North America 1991, 38: 991-1017. PMID: 1870914, DOI: 10.1016/s0031-3955(16)38164-0.ChaptersConceptsNevus depigmentosusPityriasis albaTinea versicolorAsh-leaf spotsEarly cutaneous manifestationsPotassium hydroxide examinationDestruction of melanocytesDisorders of hypopigmentationHypomelanosis of ItoAtopic diathesisCutaneous manifestationsAreas of hypopigmentationInflammatory processNeurocutaneous disorderScaly patchesProgressive disorderCommon disorderTuberous sclerosisUpper trunkVitiligoDisordersHypopigmentationP. orbiculareHypomelanosisChildren
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