| Literature DB >> 30955094 |
Solenne Correard1, Jocelyn Plassais1,2, Laëtitia Lagoutte1, Nadine Botherel1, Jean-Laurent Thibaud3, Benoît Hédan1, Laurence Richard4, Anne-Sophie Lia5, Valérie Delague6, Catherine Mège7, Stéphane Mathis8, Eric Guaguère9, Manon Paradis10, Jean-Michel Vallat4, Pascale Quignon1, Catherine André11.
Abstract
In humans, hereditary sensory neuropathies (HSN), also known as hereditary sensory and autonomic neuropathies (HSAN), constitute a clinically and genetically heterogeneous group of disorders characterized by progressive sensory loss, often accompanied by chronic skin ulcerations and nail dystrophic changes. To date, although around 20 genes have already been discovered, they do not explain the genetic causes of all patients. In dogs, similar neuropathies are also diagnosed, several breeds being predisposed to specific forms of the disease. Indeed, the breed specificity of most canine genetic diseases is due to the small numbers of founders and high levels of inbreeding. Recent knowledge and tools developed to study the canine genome efficiently allows deciphering the genetic bases of such diseases. To date, a dozen breeds are recognized to develop specific HSN. For the Border collie and hunting dog breeds, the genes involved have recently been discovered. Other affected breeds thus constitute potential genetic models, with new genes to be found in dogs that can be considered as candidate genes for human HSAN/HSN. Here, we review the different forms of human and canine HSAN/HSN and we present a novel form in Fox terrier cases, highlighting the advantages of the dog model for such rare human diseases.Entities:
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Year: 2019 PMID: 30955094 DOI: 10.1007/s00439-019-02003-x
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132