Literature DB >> 29888467

Bilateral cerebellar cysts and cerebral white matter lesions with cortical dysgenesis: Expanding the phenotype of LAMB1 gene mutations.

T Okazaki1,2, Y Saito1, T Hayashida1, S Akaboshi3, N Miyake4, N Matsumoto4, N Kasagi2, K Adachi5, Y Shinohara6, E Nanba2,5, Y Maegaki1,2.   

Abstract

LAMB1 gene analysis should be considered for intellectually disabled patients with cerebellar cysts, white matter signal change, and cortical malformation. Muscular involvement is absent, in contrast to the α-dystroglycanopathy types of congenital muscular dystrophies.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Year:  2018        PMID: 29888467     DOI: 10.1111/cge.13378

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


  2 in total

1.  A homozygous missense variant in laminin subunit beta 1 as candidate causal mutation of hemifacial microsomia in Romagnola cattle.

Authors:  Joana G P Jacinto; Irene M Häfliger; Marco Bernardini; Maria Teresa Mandara; Ezio Bianchi; Marilena Bolcato; Noemi Romagnoli; Arcangelo Gentile; Cord Drögemüller
Journal:  J Vet Intern Med       Date:  2021-11-19       Impact factor: 3.333

2.  Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation.

Authors:  Rei Yasuda; Tomokatsu Yoshida; Ikuko Mizuta; Masashi Watanabe; Masakazu Nakano; Ryuichi Sato; Yuichi Tokuda; Natsue Omi; Norio Sakai; Masanori Nakagawa; Kei Tashiro; Toshiki Mizuno
Journal:  Neurol Genet       Date:  2020-05-19
  2 in total

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