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RFC1 expansions are a common cause of idiopathic sensory neuropathy.


ABSTRACT: After extensive evaluation, one-third of patients affected by polyneuropathy remain undiagnosed and are labelled as having chronic idiopathic axonal polyneuropathy, which refers to a sensory or sensory-motor, axonal, slowly progressive neuropathy of unknown origin. Since a sensory neuropathy/neuronopathy is identified in all patients with genetically confirmed RFC1 cerebellar ataxia, neuropathy, vestibular areflexia syndrome, we speculated that RFC1 expansions could underlie a fraction of idiopathic sensory neuropathies also diagnosed as chronic idiopathic axonal polyneuropathy. We retrospectively identified 225 patients diagnosed with chronic idiopathic axonal polyneuropathy (125 sensory neuropathy, 100 sensory-motor neuropathy) from our general neuropathy clinics in Italy and the UK. All patients underwent full neurological evaluation and a blood sample was collected for RFC1 testing. Biallelic RFC1 expansions were identified in 43 patients (34%) with sensory neuropathy and in none with sensory-motor neuropathy. Forty-two per cent of RFC1-positive patients had isolated sensory neuropathy or sensory neuropathy with chronic cough, while vestibular and/or cerebellar involvement, often subclinical, were identified at examination in 58%. Although the sensory ganglia are the primary pathological target of the disease, the sensory impairment was typically worse distally and symmetric, while gait and limb ataxia were absent in two-thirds of the cases. Sensory amplitudes were either globally absent (26%) or reduced in a length-dependent (30%) or non-length dependent pattern (44%). A quarter of RFC1-positive patients had previously received an alternative diagnosis, including Sjögren's syndrome, sensory chronic inflammatory demyelinating polyneuropathy and paraneoplastic neuropathy, while three cases had been treated with immune therapies.

SUBMITTER: Curro R 

PROVIDER: S-EPMC8262986 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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RFC1 expansions are a common cause of idiopathic sensory neuropathy.

Currò Riccardo R   Salvalaggio Alessandro A   Tozza Stefano S   Gemelli Chiara C   Dominik Natalia N   Galassi Deforie Valentina V   Magrinelli Francesca F   Castellani Francesca F   Vegezzi Elisa E   Businaro Pietro P   Callegari Ilaria I   Pichiecchio Anna A   Cosentino Giuseppe G   Alfonsi Enrico E   Marchioni Enrico E   Colnaghi Silvia S   Gana Simone S   Valente Enza Maria EM   Tassorelli Cristina C   Efthymiou Stephanie S   Facchini Stefano S   Carr Aisling A   Laura Matilde M   Rossor Alexander M AM   Manji Hadi H   Lunn Michael P MP   Pegoraro Elena E   Santoro Lucio L   Grandis Marina M   Bellone Emilia E   Beauchamp Nicholas J NJ   Hadjivassiliou Marios M   Kaski Diego D   Bronstein Adolfo M AM   Houlden Henry H   Reilly Mary M MM   Mandich Paola P   Schenone Angelo A   Manganelli Fiore F   Briani Chiara C   Cortese Andrea A  

Brain : a journal of neurology 20210601 5


After extensive evaluation, one-third of patients affected by polyneuropathy remain undiagnosed and are labelled as having chronic idiopathic axonal polyneuropathy, which refers to a sensory or sensory-motor, axonal, slowly progressive neuropathy of unknown origin. Since a sensory neuropathy/neuronopathy is identified in all patients with genetically confirmed RFC1 cerebellar ataxia, neuropathy, vestibular areflexia syndrome, we speculated that RFC1 expansions could underlie a fraction of idiopa  ...[more]

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