Presentation and Diagnosis of Tuberous Sclerosis Complex in Infants

OBJECTIVES: Tuberous sclerosis complex (TSC) is a neurocutaneous genetic disorder with a high prevalence of epilepsy and neurodevelopmental disorders. TSC can be challenging to diagnose in infants because they often do not show many clinical signs early in life. In this study, we describe the timing...

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Pubblicato in:Pediatrics
Autori principali: Davis, Peter E., Filip-Dhima, Rajna, Sideridis, Georgios, Peters, Jurriaan M., Au, Kit Sing, Northrup, Hope, Bebin, E. Martina, Wu, Joyce Y., Krueger, Darcy, Sahin, Mustafa
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Academy of Pediatrics 2017
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5703775/
https://ncbi.nlm.nih.gov/pubmed/29101226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2016-4040
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