| Literature DB >> 31558336 |
Francesca Gualandi1, Elisabetta Sette2, Fernanda Fortunato3, Stefania Bigoni3, Domenico De Grandis4, Chiara Scotton3, Rita Selvatici3, Marcella Neri3, Alex Incensi5, Rocco Liguori5, Markus Storbeck6, Mert Karakaya6, Valentina Simioni2, Stefano Squarzoni7, Vincent Timmerman8, Brunhilde Wirth6, Vincenzo Donadio5, Valeria Tugnoli2, Alessandra Ferlini9.
Abstract
We describe a novel ATP7A gene mutation associated with distal motor neuropathy, mild connective tissue abnormalities and autonomic disturbances. Next-generation sequencing analysis of a lower-motor neuron diseases gene panel was performed in two sibs presenting with distal motor neuropathy plus an autonomic dysfunction, which main manifestations were retrograde ejaculation, diarrhea and hyperhydrosis. Probands underwent dysmorphological, neurological, electrophysiological as well as biochemical evaluations and somatic and autonomic innervation studies on skin biopsies. A novel missense mutation (p.A991D) was identified in the X-linked ATP7A gene, segregating in both brothers and inherited from their healthy mother. Biochemical studies on patients' blood samples showed reduced serum copper and ceruloplasmin levels. Clinical and neurophysiological evaluation documented dysautonomic signs. Quantitative evaluation of skin innervation disclosed a small fiber neuropathy with prevalent autonomic involvement. Mutations in the ATP7A gene, encoding for a copper-transporting ATPase, have been associated with the severe infantile neurodegenerative Menkes disease and in its milder variant, the Occipital Horn Syndrome. Only two ATP7A mutations were previously reported as causing, a pure axonal distal motor neuropathy (dHMN-SMAX3). The phenotype we report represents a further example of this rare genotype-phenotype correlation and highlights the possible occurrence in SMAX3 of autonomic disturbances, as described for Menkes disease and Occipital Horn Syndrome.Entities:
Keywords: ATP7A mutation; Autonomic neuropathy; Peripheral neuropathy
Year: 2019 PMID: 31558336 DOI: 10.1016/j.nmd.2019.08.008
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296