
Congenital or infantile autosomal recessive optic atrophy is rare. The autosomal recessive syndrome of optic atrophy associated with diabetes is less rare. Dominant juvenile optic atrophy occurs frequently. Behr's heredo-familial optic atrophy, with its neurological mainfestations and its recessive autosomal inheritance, is rare. Sex-linked optic atrophy is exceptional. Leber's optic neuritis occurs frequently. Its heredity is apparently sex-linked, but no classical mode of transmission can be applied. Cytoplasmic heredity is the most probable.
Male, Optic Neuritis, Sex Chromosomes, Extrachromosomal Inheritance, Genes, Recessive, Syndrome, Pedigree, Diabetes Complications, Optic Atrophy, Diabetic Neuropathies, Gene Frequency, Humans, Female, Diabetes Insipidus, Genes, Dominant
Male, Optic Neuritis, Sex Chromosomes, Extrachromosomal Inheritance, Genes, Recessive, Syndrome, Pedigree, Diabetes Complications, Optic Atrophy, Diabetic Neuropathies, Gene Frequency, Humans, Female, Diabetes Insipidus, Genes, Dominant
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