Noonan Syndrome in Thai Children

Nonglak Boonchooduang, Orawan Louthrenoo & Pranoot Tanpaiboon

Indian Pediatrics , Volume 57, Issue 10, 1 October 2020, Pages 967-968 , JIF=1.186

คลิกเพื่อดูข้อมูลผลงานตีพิมพ์

This study describes clinical features of Noonan syndrome and gene mutations, including PTPN11, SOS1, and BRAF in the Thai population. Widely spaced eyes were the most common finding from the digital facial analysis technology used in this study.