Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning to read despite adequate intelligence, education, and environment, and normal senses.
The genetic etiology of dyslexia is heterogeneous and found on chromosomes 2, 3, 6, 15, and 18.
At this time no mutation seems to be seen on these areas but it is genetic and found in families.
Chromosome 9.
chromosome 19
Any chromosome can be affected by aneuploidy. However, generally, the larger the chromosome, the larger the likelihood that the change in chromosome number will be fatal.
Chromosome 13
x
*affected
Too many
It's Chromosome X .
Chromosome 21q22 which accounts for 20% of familial ALS.
The population affected is females. The chromosome that this affects is on the X chromosome which is the sex chromosome that females carry. This affects 1 in every 2,500 live births.
if you mean chromosome its the 15th......
13