Sjogren's syndrome.. Unusual human hereditary genetic hereditary disease inherited as an autosomal recessive. Nostalgia is spastic. Retardation. Speech abnormalities. Two Colodonians

Sjogren's syndrome:
- Unusual human neuropathic hereditary skin disease, inherited as an autosomal recessive.
Clinical manifestations:
- Skin disorder becomes apparent after the first few months of life.
- Skin manifestations are characterized by excessive lesions of horny, pubic, floral color.
- Neurophysiological manifestations: such as spastic necrosis of spasticity mental retardation abnormalities in speech epilepsy and descriptive degenerative degeneration.
- Some of the infected children are born Colodione boys.