lissencephaly type 3-familial fetal akinesia sequence syndrome
MONDO:0019449Mondo
Findings
No curated finding names lissencephaly type 3-familial fetal akinesia sequence syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Lissencephaly type 3-familial fetal akinesia sequence syndrome is characterized by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia.
Definition from the Mondo Disease Ontology (MONDO:0019449), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of