Lissencephaly type 3 - familial fetal akinesia sequence (Q88646): Difference between revisions
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Síndrome da sequência de lissencefalia tipo 3 - acinesia fetal familiar é caracterizada pela associação de microencefalia, agenesia do corpo caloso, hipoplasia de tronco encefálico, cerebelo cístico e sequência de acinesia fetal. | |||
| description / en | description / en | ||
Lissencephaly type 3 - familial fetal akinesia sequence syndrome is characterised by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. | |||
Revision as of 14:58, 15 August 2026
Lissencephaly type 3 - familial fetal akinesia sequence syndrome is characterised by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_958288618 |
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| English | Lissencephaly type 3 - familial fetal akinesia sequence |
Lissencephaly type 3 - familial fetal akinesia sequence syndrome is characterised by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. |
