Dataset Information

Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in TRAPPC9 Gene and Literature Review.

ABSTRACT:

Objective

Pathogenic mutations of the TRAPPC9 gene are the rare genetic causes of autosomal recessive intellectual disability (ID). There are several features that are not fully penetrant such as microcephaly, dysmorphic facial features, obesity, autism spectrum disorder (ASD), attention-deficit hyperactivity disorder (ADHD), and brain abnormalities in TRAPPC9 mutations.

Methods

We performed whole-exome sequencing to evaluate 2 Turkish siblings with ASD and ID born to healthy and consanguineous parents. Parental samples were also analyzed, specifically targeting variants detected in these patients.

Results

We present a novel homozygous mutation in the TRAPPC9 gene, c.484G>T (p.Glu162Ter). Additionally, we aim to provide a more comprehensive understanding of the clinical features of a novel homozygous TRAPPC9 mutation. In addition to ID, the siblings in this report suffered from ASD and specific stereotypes as hand-flapping behavior.

Conclusion

Although there are inconsistencies in the presentation of ASD in TRAPPC9 mutations, repetitive behaviors (hand-flapping) were typical in our cases and several previous reports. The current mutation was described to cause a homozygous premature termination codon that resulted in the absence of the TRAPPC9 protein. We suggest that TRAPPC9 mutations are not only related to ID but also to ASD and hand-flapping behaviors.

SUBMITTER: Bolat H

PROVIDER: S-EPMC9421696 | biostudies-literature | 2022 Jul

REPOSITORIES: biostudies-literature

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Publications

Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in <i>TRAPPC9</i> Gene and Literature Review.

Bolat Hilmi H Ünsel-Bolat Gül G Derin Hatice H Şen Aşkın A Ceylaner Serdar S

Molecular syndromology 20220309 4

<h4>Objective</h4>Pathogenic mutations of the <i>TRAPPC9</i> gene are the rare genetic causes of autosomal recessive intellectual disability (ID). There are several features that are not fully penetrant such as microcephaly, dysmorphic facial features, obesity, autism spectrum disorder (ASD), attention-deficit hyperactivity disorder (ADHD), and brain abnormalities in <i>TRAPPC9</i> mutations.<h4>Methods</h4>We performed whole-exome sequencing to evaluate 2 Turkish siblings with ASD and ID born t ...[more]

PMID: 36158060

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