Tuberous sclerosis complex: a case report

Background. Tuberous sclerosis complex (TSC) is a rare genetic disorder diagnosed in 6000-10000 children annually, marked by hamartomas in various organs due to hyperactivity of the mTOR pathway. Case report. A 9-year-old male with TSC exhibited developmental delays, skin lesions, vision and hearing...

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Bibliographic Details
Main Authors: Hanna Sebesi, Réka Borka-Balás, Micheu Cristian Ion
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2024-09-01
Series:Romanian Journal of Pediatrics
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Online Access:https://rjp.com.ro/articles/2024.3/RJP_2024_3_Art-08.pdf
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