feb 7, 1894 - Apert syndrome - acrocephalosyndactyly I
Description:
It is named after Eugene Apert, French physician, in 1906 although some reports suggest it was first described by Wheatondefect on the fibroblast growth factor receptor 2 (FGFR2) gene, located on chromosome 10q26.
Added to timeline:
Date:
feb 7, 1894
Now
~ 131 years ago