TUBEROUS SCLEROSIS COMPLEX
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Abstract
Tuberous sclerosis complex is an autosomal dominant genetic disorder that affects multiple systems, resulting in the formation of hamartomas in different organs such as the skin, central nervous system, kidneys, and lungs. This leads to a variety of symptoms, ranging from seizures to skin manifestations. Here, we report a case of a 14-year-old male child who presented with myoclonic fits and fever. He was eventually diagnosed to be suffering from tuberous sclerosis, based on his clinical signs and investigations.
KEYWORDS: Fever, Seizures, Hamartomas, Tuberous Sclerosis
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