Causes of Apert Syndrome:- Apert syndrome is a rare genetic disorder caused by a mutation in the FGFR2 gene, which controls bone development.- This gene mutation disrupts the timing of bone fusion ...
A UK woman who says she was abandoned at birth due to a rare genetic condition has devoted her life to caring for her son, Elijah, who has the same affliction. “My philosophy in life is you can either ...
MADISONVILLE, Texas (KBTX) - The Madisonville Consolidated Independent School District hosted a volleyball tournament to support Waylon, a one-year-old facing the challenges of Apert Syndrome. Waylon ...
This image shows craniofacial growth patterns in mouse models for Apert syndrome. Apert syndrome is caused by two neighboring mutations on Fibroblast growth factor receptor 2 (FGFR2). Multimodal ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback