| Literature DB >> 31420593 |
Fulya Akçimen1, Atay Vural2, Hacer Durmuş3, Arman Çakar3, Henry Houlden4, Yeşim G Parman3, A Nazlı Başak5.
Abstract
Distal hereditary motor neuronopathies (dHMN) are a genetically heterogeneous group of neuromuscular disorders caused by anterior horn cell degeneration and progressive distal muscle weakness. A heterozygous missense variant in FBXO38 has been previously described in two families affected by autosomal-dominant dHMN. In this paper, we describe a homozygous missense variant in FBXO38 (c.1577G>A; p.(Arg526Gln)) in a young Turkish female, offspring of consanguineous parents, with a congenital mild neuronopathy with idiopathic toe walking, normal sensory examination, and hearing loss. This work is the first to describe a novel homozygous variant and a suggested loss of function mechanism in FBXO38, expanding the dHMN type IID phenotype.Entities:
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Year: 2019 PMID: 31420593 DOI: 10.1038/s10038-019-0652-y
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172