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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Pediatrics
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Academy of Pediatrics 2017
Pynciau:
Article
Mynediad Ar-lein: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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