Griffin J R
Southern California College of Optometry, Fullerton.
Optom Vis Sci. 1992 Feb;69(2):148-51. doi: 10.1097/00006324-199202000-00008.
The nine pedigrees presented here suggest an autosomal dominant mode of transmission for the dyseidetic type of dyslexia. Sex-influence probably accounts for the high male to female ratio. Other modes of transmission are highly unlikely for dyseidesia but possible for other types of dyslexia, with the multifactorial mode being most likely. Genetic counseling is particularly feasible in cases of dyseidetic dyslexia.
此处展示的九个谱系表明，发育性诵读困难的视觉性失读类型呈常染色体显性遗传模式。性别影响可能是导致男性与女性比例偏高的原因。其他遗传模式对于视觉性失读症来说极不可能，但对于其他类型的诵读困难则有可能，其中多因素模式最为可能。在视觉性失读症病例中，遗传咨询尤为可行。
