Genetics of syndromic and non-syndromic hereditary nail disorders

dc.contributor.authorBergqvist, Christina
dc.contributor.authorRamia, Paul S.
dc.contributor.authorAbbas, Ossama M.
dc.contributor.authorKurban, Mazen S.
dc.contributor.departmentDermatology
dc.contributor.departmentInternal Medicine
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:40:44Z
dc.date.available2025-01-24T11:40:44Z
dc.date.issued2017
dc.description.abstractThe nail is a unique epithelial skin appendage made up of a fully keratinized nail plate. The nail can be affected in several systemic illnesses, dermatological diseases, and inherited nail disorders. Nail dystrophies can present as isolated disorders or as a part of syndromes. Substantial progress has been achieved in the management and diagnosis of nail diseases; however, not much is known about the underlying molecular controls of nail growth. The homeostasis and development of the nail appendage depend on the intricate interactions between the epidermis and underlying mesenchyme, and comprise different signaling pathways such as the WNT signaling pathway. Digit-tip regeneration in mice and humans has been a known fact for the past six decades; however, only recently the underlying biological mechanisms by which the nail organ achieves digit regeneration have been elucidated. Moreover, significant progress has been made in identifying nail stem cells and localizing stem cell niches in the nail unit. More fascinating, however, is the role they play in orchestrating the processes that lead to the regeneration of the digit. Further elucidating the role of nail stem cells and the signaling pathways driving epithelial–mesenchymal interactions in the nail unit might contribute to the development of novel therapeutic tools for amputees. © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
dc.identifier.doihttps://doi.org/10.1111/cge.12852
dc.identifier.eid2-s2.0-85006511316
dc.identifier.pmid27613389
dc.identifier.urihttp://hdl.handle.net/10938/29551
dc.language.isoen
dc.publisherBlackwell Publishing Ltd
dc.relation.ispartofClinical Genetics
dc.sourceScopus
dc.subjectHereditary nail disorders
dc.subjectLimb regeneration
dc.subjectNon-syndromic nail disorders
dc.subjectSyndromic nail disorders
dc.subjectAnimals
dc.subjectCell differentiation
dc.subjectEpidermis
dc.subjectHomeostasis
dc.subjectHumans
dc.subjectMesoderm
dc.subjectMice
dc.subjectNail diseases
dc.subjectNails
dc.subjectRegeneration
dc.subjectStem cell niche
dc.subjectWnt signaling pathway
dc.subjectBone morphogenetic protein
dc.subjectEnzyme
dc.subjectKeratin
dc.subjectNotch receptor
dc.subjectTumor necrosis factor
dc.subjectWnt protein
dc.subjectEmbryology
dc.subjectGenetic disorder
dc.subjectHuman
dc.subjectLimb development
dc.subjectMorphogenesis
dc.subjectNail disease
dc.subjectNail dysplasia
dc.subjectNonhuman
dc.subjectPriority journal
dc.subjectReview
dc.subjectStem cell
dc.subjectSyndrome
dc.subjectAnimal
dc.subjectGenetics
dc.subjectGrowth, development and aging
dc.subjectMouse
dc.subjectNail
dc.subjectPathology
dc.subjectPathophysiology
dc.subjectWnt signaling
dc.titleGenetics of syndromic and non-syndromic hereditary nail disorders
dc.typeReview

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