| Literature DB >> 29882456 |
Alexander Conant1, Julian Curiel2, Amy Pizzino1, Parisa Sabetrasekh1, Jennifer Murphy3, Miriam Bloom4, Sarah H Evans5, Guy Helman1,6,7, Ryan J Taft8,9, Cas Simons7,9, Matthew T Whitehead10,11, Steven A Moore12, Adeline Vanderver1,2,3,11.
Abstract
Leukodystrophies and genetic leukoencephalopathies are a heterogeneous group of heritable disorders that affect the glial-axonal unit. As more patients with unsolved leukodystrophies and genetic leukoencephalopathies undergo next generation sequencing, causative mutations in genes leading to central hypomyelination are being identified. Two such individuals presented with arthrogryposis multiplex congenita, congenital hypomyelinating neuropathy, and central hypomyelination with early respiratory failure. Whole exome sequencing identified biallelic mutations in the CNTNAP1 gene: homozygous c.1163G>C (p.Arg388Pro) and compound heterozygous c.967T>C (p.Cys323Arg) and c.319C>T (p.Arg107*). Sural nerve and quadriceps muscle biopsies demonstrated progressive, severe onion bulb and axonal pathology. By ultrastructural evaluation, septate axoglial paranodal junctions were absent from nodes of Ranvier. Serial brain magnetic resonance images revealed hypomyelination, progressive atrophy, and reduced diffusion in the globus pallidus in both patients. These 2 families illustrate severe progressive peripheral demyelinating neuropathy due to the absence of septate paranodal junctions and central hypomyelination with neurodegeneration in CNTNAP1-associated arthrogryposis multiplex congenita.Entities:
Keywords: Boylan-Dew-Greco syndrome; Caspr1; hypomyelination; lethal congenital contracture syndrome 7; leukodystrophy; myelin; pathology; whole exome sequencing
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Year: 2018 PMID: 29882456 PMCID: PMC6800098 DOI: 10.1177/0883073818776157
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987