X-linked neurodegenerative syndrome, Bertini type

X-linked neurodegenerative syndrome, Bertini type is characterized by generalized hypotonia, psychomotor deficit, congenital ataxia and recurrent bronchopulmonary infections. It has been described in seven males from three generations of a family. Five of them died during the first years of life and the remaining patients developed myoclonic encephalopathy and macular degeneration. The locus has been mapped to Xp22.33-pter.

0 clinical trials for this condition and its sub-types, 0 tagged with X-linked neurodegenerative syndrome, Bertini type itself.