Related Experiment Video
Updated: Jul 10, 2025

Author Spotlight: Collecting the Brain and Serum from the Same Mice Fetus to Study Brain Tumor Development
Published on: May 17, 2024
A case of infantile spasms with three possibly pathogenic de novo missense variants in NF1 and GABBR1
Kazuki Watanabe1, Kazuo Kubota2,3, Mitsuko Nakashima4
1Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Abstract:
Neurofibromatosis type 1 (NF1) is one of the most common hereditary neurocutaneous disorders. Here, we report a unique case of a patient with typical NF1 findings and infantile spasms who had three possibly pathogenic de novo variants, c.3586C>T, p.(Leu1196Phe) and c.3590C>T, p.(Ala1197Val) in NF1 located in cis and c.1042G>C, p.(Ala348Pro) in GABBR1. This study contributes to our understanding of the effect of two cis variants on NF1 phenotypes and GABBR1-related neuropsychiatric disorders.
More Related Videos
Related Concept Videos
Neurulation
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
NF-κB-dependent Signaling Pathway
NF-κB-dependent Signaling Mechanism
The...
Inborn Errors of Metabolism
Mutations

