Ontology highlight
ABSTRACT:
SUBMITTER: Hamel BC
PROVIDER: S-EPMC1734300 | biostudies-other | 1999 Feb
REPOSITORIES: biostudies-other
Hamel B C BC Wesseling P P Renier W O WO van den Helm B B Ropers H H HH Kremer H H Mariman E C EC
Journal of medical genetics 19990201 2
We report on a family with an X linked neurodegenerative disorder consisting of mental retardation, blindness, convulsions, spasticity, and early death. Neuropathological examination showed mild hypomyelination. By linkage analysis, the underlying genetic defect could be assigned to the pericentromeric region of the X chromosome with a maximum lod score of 3.30 at theta=0.0 for the DXS1204 locus with DXS337 and PGK1P1 as flanking markers. ...[more]