Poor Mental Development in Patients With Tuberous Sclerosis Complex

Abstract
TUBEROUS SCLEROSIS complex (TSC) is characterized pathologically as hamartias (nongrowing focal congenital anomalies), hamartomas (benign growths), and true neoplasms1 in various organs, such as brain, skin, kidneys, liver, and heart.2 The predominant neurological manifestations of TSC are seizures, mental retardation, and behavioral abnormalities, with seizures being the most common initial sign of central nervous system involvement.3 Poorly controlled seizures as well as certain types of seizures, eg, infantile spasms, are considered to be indicative of poor overall neurodevelopmental prognosis.3,4 Some of the other alleged risk factors include male sex5 and exposure to diphtheria, tetanus, and pertussis (DTP) immunizations.6

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