Identification of Missense <i>ADGRV1</i> Mutation as a Candidate Genetic Cause of Familial Febrile Seizure 4

Febrile seizure (FS) is related to a febrile illness (temperature > 38 °C) not caused by an infection of central nervous system, without neurologic deficits in children aged 6-60 months. The family study implied a polygenic model in the families of proband(s) with single FS, however in families w...

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Main Authors: Ji Yoon Han (Author), Hyun Joo Lee (Author), Young-Mock Lee (Author), Joonhong Park (Author)
Format: Book
Published: MDPI AG, 2020-09-01T00:00:00Z.
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001 doaj_039a9cc9b32446dc8cd9c7f76f3241e6
042 |a dc 
100 1 0 |a Ji Yoon Han  |e author 
700 1 0 |a Hyun Joo Lee  |e author 
700 1 0 |a Young-Mock Lee  |e author 
700 1 0 |a Joonhong Park  |e author 
245 0 0 |a Identification of Missense <i>ADGRV1</i> Mutation as a Candidate Genetic Cause of Familial Febrile Seizure 4 
260 |b MDPI AG,   |c 2020-09-01T00:00:00Z. 
500 |a 10.3390/children7090144 
500 |a 2227-9067 
520 |a Febrile seizure (FS) is related to a febrile illness (temperature > 38 °C) not caused by an infection of central nervous system, without neurologic deficits in children aged 6-60 months. The family study implied a polygenic model in the families of proband(s) with single FS, however in families with repeated FS, inheritance was matched to autosomal dominance with reduced disease penetrance. A 20 month-old girl showed recurrent FS and afebrile seizures without developmental delay or intellectual disability. The seizures disappeared after 60 months without anti-seizure medication. The 35 year-old proband's mother also experienced five episodes of simple FS and two episodes of unprovoked seizures before 5 years old. Targeted exome sequencing was conducted along with epilepsy/seizure-associated gene-filtering to identify the candidate causative mutation. As a result, a heterozygous c.2039A>G of the <i>ADGRV1</i> gene leading to a codon change of aspartic acid to glycine at the position 680 (rs547076322) was identified. This protein's glycine residue is highly conserved, and its allele frequency is 0.00002827 in the gnomAD population database. <i>ADGRV1</i> mutation may have an influential role in the occurrence of genetic epilepsies, especially those with febrile and afebrile seizures. Further investigation of <i>ADGRV1</i> mutations is needed to prove that it is a significant susceptible gene for febrile and/or afebrile seizures in early childhood. 
546 |a EN 
690 |a <i>ADGRV1</i> mutation 
690 |a familial febrile seizure 4 
690 |a afebrile seizure 
690 |a febrile seizure 
690 |a targeted exome sequencing 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Children, Vol 7, Iss 9, p 144 (2020) 
787 0 |n https://www.mdpi.com/2227-9067/7/9/144 
787 0 |n https://doaj.org/toc/2227-9067 
856 4 1 |u https://doaj.org/article/039a9cc9b32446dc8cd9c7f76f3241e6  |z Connect to this object online.