SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.
Katharina VillWolfgang Müller-FelberDieter GläserMarius KuhnVeronika TeuschHerbert SchreiberJoachim WeisJörg KlepperAnja SchirmacherAstrid BlaschekManuela WiessnerTim M StromBianca DrägerKristina Hofmeister-KiltzMoritz TackeLucia GerstlPeter YoungRita HorvathJan SenderekPublished in: Human genetics (2018)
Mutations in the SACS gene have been initially reported in a rare autosomal recessive cerebellar ataxia syndrome featuring prominent cerebellar atrophy, spasticity and peripheral neuropathy as well as retinal abnormalities in some cases (autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS). In the past few years, the phenotypic spectrum has broadened, mainly owing to the availability and application of high-throughput genetic testing methods. We identified nine patients (three sib pairs, three singleton cases) with isolated, non-syndromic hereditary motor and sensory neuropathy (HMSN) who carried pathogenic SACS mutations, either in the homozygous or compound heterozygous state. None of the patients displayed spasticity or pyramidal signs. Ataxia, which was noted in only three patients, was consistent with a sensory ataxia. Nerve conduction and nerve biopsy studies showed mixed demyelinating and axonal neuropathy. Brain MRI scans were either normal or revealed isolated upper vermis atrophy of the cerebellum. Our findings confirm the broad clinical spectrum associated with SACS mutations, including pure polyneuropathy without characteristic clinical and brain imaging manifestations of ARSACS.
Keyphrases
- end stage renal disease
- newly diagnosed
- ejection fraction
- early onset
- chronic kidney disease
- spinal cord injury
- high throughput
- peritoneal dialysis
- computed tomography
- multiple sclerosis
- magnetic resonance
- single cell
- patient reported outcomes
- botulinum toxin
- case report
- brain injury
- diabetic retinopathy
- dna methylation
- optical coherence tomography
- genome wide
- gestational age
- blood brain barrier
- transcription factor
- genome wide analysis
- birth weight