Lethal olivopontoneocerebellar hypoplasia with dysmorphic features in sibs.
case_report · Level V
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- Record sourced from PubMed, PMID 1433235.
- Also identified by PMC identifier 1016134.
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Abstract
This report describes the clinical and neuropathological features in male and female sibs who died shortly after birth as a result of frequent convulsions and lack of spontaneous respiratory effect. Both sibs had a prominent occiput with mild contractures and the female also had overlapping fingers and rockerbottom feet. The genetic and neuropathological findings were consistent with a diagnosis of an autosomal recessive form of olivopontoneocerebellar hypoplasia/atrophy.
Medical subject headings
- Abnormalities, Multiple
- Microcephaly
- Micrognathism
- Olivopontocerebellar Atrophies
- Polyhydramnios