Miller-Dieker syndrome (Q86804): Difference between revisions
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A síndrome de Miller-Dieker é uma síndrome de deleção de gene contíguo do cromossomo 17p13.3, caracterizada por lissencefalia clássica (lissencefalia tipo 1) e características faciais distintas. | |||
| description / en | description / en | ||
Miller-Dieker Syndrome is a contiguous gene deletion syndrome of chromosome 17p13.3, characterised by classical lissencephaly (lissencephaly type 1) and distinct facial features. | |||
Revision as of 12:21, 15 August 2026
Miller-Dieker Syndrome is a contiguous gene deletion syndrome of chromosome 17p13.3, characterised by classical lissencephaly (lissencephaly type 1) and distinct facial features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_478783491 |
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| English | Miller-Dieker syndrome |
Miller-Dieker Syndrome is a contiguous gene deletion syndrome of chromosome 17p13.3, characterised by classical lissencephaly (lissencephaly type 1) and distinct facial features. |
