Lissencephaly type 3 - metacarpal bone dysplasia (Q88655): Difference between revisions
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Síndrome de lissencefalia tipo 3 - displasia óssea metacarpal é caracterizada por microcefalia grave, agiria, agenesia do corpo caloso, hipoplasia cerebelar, dismorfologia facial e pontilhado epifisário dos ossos metacarpais. | |||
| description / en | description / en | ||
Lissencephaly type 3 - metacarpal bone dysplasia syndrome is characterised by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones. | |||
Revision as of 14:59, 15 August 2026
Lissencephaly type 3 - metacarpal bone dysplasia syndrome is characterised by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_807545724 |
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| English | Lissencephaly type 3 - metacarpal bone dysplasia |
Lissencephaly type 3 - metacarpal bone dysplasia syndrome is characterised by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones. |
