Genomic coordinate (human 3:70,954,693 FOXP1) & (human 7:114,086,327 FOXP2).
Cytoband (human 3p13 FOXP1) & (human 7q31.1 FOXP2).
OMIM’genes = 15 @ 3p13 & 72 @ 7q31.1
Polymorphs= 772 FOXP1 & 317 FOXP2.
Here I 🎁 present: “FOXP1 & FOXP2 in Dyspraxia“, Victor McKusick, Mendelian Inheritance in Man’, 1966.
INTRODUCTION.
Dyspraxia, also known as Developmental Coordination Disorder (DCD), is a chronic neurodevelopmental condition that affects motor coordination, balance, and spatial awareness. Though unrelated to intelligence, it impacts the brain’s ability to plan, organize, and execute physical movements, affecting everything from tying shoelaces and handwriting to speech and multi-step tasks.
