Literature DB >> 33639934

Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia.

Carla De Angelis1,2, Alicia B Byrne3,4, Hamish S Scott3,5,2,4,6, Christopher Barnett7,8,9, Rebecca Morrow3, Jinghua Feng5,4, Thuong Ha3,5, Paul Wang5, Andreas W Schreiber5,4,10, Milena Babic3, Ajay Taranath11,2, Nick Manton12, Sarah L King-Smith3,6, Quenten Schwarz13,4, Peer Arts3.   

Abstract

BACKGROUND: Periventricular nodular heterotopia (PNH) is a malformation of cortical development characterized by nodules of abnormally migrated neurons. The cause of posteriorly placed PNH is not well characterised and we present a case that provides insights into the cause of posterior PNH. CASE
PRESENTATION: We report a fetus with extensive posterior PNH in association with biallelic variants in LAMC3. LAMC3 mutations have previously been shown to cause polymicrogyria and pachygyria in the occipital cortex, but not PNH. The occipital location of PNH in our case and the proposed function of LAMC3 in cortical development suggest that the identified LAMC3 variants may be causal of PNH in this fetus.
CONCLUSION: We hypothesise that this finding extends the cortical phenotype associated with LAMC3 and provides valuable insight into genetic cause of posterior PNH.

Entities:  

Keywords:  Case report; LAMC3; Lobe; Occipital; Periventricular nodular heterotopia

Year:  2021        PMID: 33639934      PMCID: PMC7916305          DOI: 10.1186/s12920-021-00911-4

Source DB:  PubMed          Journal:  BMC Med Genomics        ISSN: 1755-8794            Impact factor:   3.063


  25 in total

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