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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Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Amaltea Medical Publishing House
2024-09-01
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Series: | Romanian Journal of Pediatrics |
Subjects: | |
Online Access: | https://rjp.com.ro/articles/2024.3/RJP_2024_3_Art-08.pdf |
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