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A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene.
- Source :
-
Clinical Case Reports . Dec2021, Vol. 9 Issue 12, p1-5. 5p. - Publication Year :
- 2021
-
Abstract
- Reelinopathies cause a distinctive lissencephaly type associated with cerebellar hypoplasia. To help further management, we wanted to report here the first prenatal diagnosis due to a homozygous inherited reelinopathy. [ABSTRACT FROM AUTHOR]
- Subjects :
- *GENETIC mutation
*PRENATAL diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 20500904
- Volume :
- 9
- Issue :
- 12
- Database :
- Academic Search Index
- Journal :
- Clinical Case Reports
- Publication Type :
- Academic Journal
- Accession number :
- 154347323
- Full Text :
- https://doi.org/10.1002/ccr3.4882