Literature DB >> 29797509

PRUNE1-related disorder: Expanding the clinical spectrum.

E Imagawa1, Y Yamamoto1, S Mitsuhashi1, B Isidor2, T Fukuyama3, M Kato4, M Sasaki5, S Tanabe6, S Miyatake1, T Mizuguchi1, A Takata1, N Miyake1, N Matsumoto1.   

Abstract

Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies (NMIHBA) (OMIM #617481) is an autosomal recessive disease characterized by progressive microcephaly, plagiocephaly, hypotonia, spastic quadriparesis, global developmental delay, intellectual disability, optic features and abnormal brain magnetic resonance imaging (MRI). NMIHBA was recently reported to be caused by PRUNE1 mutations. Eight mutations have been reported in 13 unrelated families. Here, we report 3 PRUNE1 mutations in 1 Caucasian and 3 Japanese families. One recurrent missense mutation (p.Asp106Asn) was previously reported in Turkish and Italian families, while the other 2 mutations (p.Leu18Serfs*8 and p.Cys180*) are novel. We also show that mutant PRUNE1 mRNA can be subject to nonsense-mediated mRNA decay. The patients presented in this study showed atypical NMIHBA phenotypes with no progressive microcephaly. Furthermore, one Caucasian case had significant macrocephaly; therefore, patients with PRUNE1 mutations can exhibit a broad and heterogeneous spectrum of phenotypes.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  PRUNE1; microcephaly; nonsense-mediated mRNA decay; whole-exome sequencing

Mesh:

Substances:

Year:  2018        PMID: 29797509     DOI: 10.1111/cge.13385

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

1.  Identifying Candidate Genes Associated with Sporadic Amyotrophic Lateral Sclerosis via Integrative Analysis of Transcriptome-Wide Association Study and Messenger RNA Expression Profile.

Authors:  Ping Li; Shiqiang Cheng; Yan Wen; Bolun Cheng; Li Liu; Xiuhua Wu; Xiang Ao; Zucheng Huang; Congrui Liao; Shaen Li; Feng Zhang; Zhongmin Zhang
Journal:  Cell Mol Neurobiol       Date:  2022-01-17       Impact factor: 5.046

2.  High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population.

Authors:  Tadahiro Mitani; Sedat Isikay; Alper Gezdirici; Elif Yilmaz Gulec; Jaya Punetha; Jawid M Fatih; Isabella Herman; Gulsen Akay; Haowei Du; Daniel G Calame; Akif Ayaz; Tulay Tos; Gozde Yesil; Hatip Aydin; Bilgen Geckinli; Nursel Elcioglu; Sukru Candan; Ozlem Sezer; Haktan Bagis Erdem; Davut Gul; Emine Demiral; Muhsin Elmas; Osman Yesilbas; Betul Kilic; Serdal Gungor; Ahmet C Ceylan; Sevcan Bozdogan; Ozge Ozalp; Salih Cicek; Huseyin Aslan; Sinem Yalcintepe; Vehap Topcu; Yavuz Bayram; Christopher M Grochowski; Angad Jolly; Moez Dawood; Ruizhi Duan; Shalini N Jhangiani; Harsha Doddapaneni; Jianhong Hu; Donna M Muzny; Dana Marafi; Zeynep Coban Akdemir; Ender Karaca; Claudia M B Carvalho; Richard A Gibbs; Jennifer E Posey; James R Lupski; Davut Pehlivan
Journal:  Am J Hum Genet       Date:  2021-09-28       Impact factor: 11.025

3.  Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene.

Authors:  Mehdi Agha Gholizadeh; Mina Mohammadi-Sarband; Fatemeh Fardanesh; Masoud Garshasbi
Journal:  BMC Med Genomics       Date:  2022-04-04       Impact factor: 3.063

  3 in total

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