Two patients with Apert syndrome with different mutations: the importance of early diagnosis
Makaleler > Tam Makale · 2018
Yazarlar: Esra IŞIK, Tahir ATİK, HÜSEYİN ONAY, Feriştah Ferda ÖZKINAY
Türk Pediatri Arşivi, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Scopus, 2018, cilt 52, ss 231-235
DOI: 10.5152/turkpediatriars.2016.3305
Özet
gene. Case-1 underwent surgery for craniosynostosis at age 10 months and he was developmentally normal during the 2 year follow-up period. As a conclusion, early surgical intervention should be considered in cases of Apert syndrome to prevent intellectual disability.