Neurocutaneous Disorders in Children
Type de ressource
Auteurs/contributeurs
- Korf, Bruce R. (Auteur)
- Bebin, E. Martina (Auteur)
Titre
Neurocutaneous Disorders in Children
Résumé
Neurofibromatosis (NF), including type 1 (NF1), type 2 (NF2), and schwannomatosis; tuberous sclerosis complex (TSC); and Sturge-Weber syndrome are 3 neurocutaneous disorders that typically present in childhood. Early recognition by the pediatrician can be critical to surveillance for treatable complications and genetic counseling. These conditions are diagnosed clinically, but genetic testing is available to clarify an uncertain diagnosis or help with genetic counseling. Although many of the complications can only be treated symptomatically, advances in understanding of the pathogenesis are opening new approaches to molecularly targeted therapeutics, which promise to alter the natural history of the conditions in the years to come.
Publication
Pediatrics in Review
Volume
38
Numéro
3
Pages
119-128
Date
2017-03
Abrév. de revue
Pediatr Rev
Langue
eng
ISSN
1526-3347
Catalogue de bibl.
PubMed
Extra
PMID: 28250072
Lien
Référence
Korf, B. R., & Bebin, E. M. (2017). Neurocutaneous Disorders in Children. Pediatrics in Review, 38(3), 119–128. https://doi.org/10.1542/pir.2015-0118
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