Jovana ima neurorazvojni poremećaj koji karakteriše usporen razvoj govora: Potrebna je pomoć ljudi dobre volje
Jovani Stevanović (16) je genetskim ispitivanjem ustanovljen neurorazvojni poremećaj sa usporenim razvojem govora i varijabilnim kognitivnim smetnjama uzrokovan haploinsuficijencijom u genu GABBR1 (kodira protein za GABA neurotransmiter). Bolest se karakteriše opstipacijom i skoliozom pored kognitivnih smetnji.
TL;DR
- Jovani Stevanović, 16, diagnosed with a neurodevelopmental disorder affecting speech and cognition due to GABBR1 gene haploinsufficiency.
- Associated conditions include constipation, scoliosis, and kphosis, which are worsening.
- Requires ongoing psychological and speech therapy treatments.
- High treatment costs necessitate public donations.
- Funds are needed for treatments in Serbia and abroad, spinal surgery, examinations, therapies, rehabilitation, and related expenses.
- Total estimated cost for treatment is 11,092,000 dinars.
- Donation methods include SMS, bank transfer, and QR code payment via the 'Budi human' foundation.