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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Vydáno v:Pediatrics
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: American Academy of Pediatrics 2017
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Article
On-line přístup: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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