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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004
See this aricle in Pubmed
Article Abstract
IBSN maps to the chromosomal region 19q13.32-13.41. The presence of a common haplotype in all the patients suggests that the disease is caused by a single mutation derived from a single ancestral founder in all the families.
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basal ganglia,lesion of
basal ganglia,lesion,bilateral
choreoathetosis
chromosomal abnormality
chromosome 19
dystonia
failure to thrive
genetic neurologic disorders
infantile bilateral striatal necrosis
nystagmus
optic atrophy
striatum,lesion of
striatum,lesion of,bilateral
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