clinical features
Last reviewed 10/2023
Majority of patients (about 75%) present with typical Friedreich's ataxia:
- mean age of onset of symptoms is 10 to 15 years
- neurologic manifestations
- gait ataxia
- earliest symptom in vast majority of patients
- limb ataxia
- is an early feature of the disease
- result in difficulty with handwriting, washing, dressing, use of cutlery and carrying drinks or food
- absent lower limb reflexes
- is an early sign present in almost all patients and reflects the underlying peripheral neuropathy.
- weakness and wasting
- a relatively late sign
- more prominent in the lower limbs compared to the upper limbs
- peripheral sensory neuropathy
- reduced/absent vibration sense and proprioception
- spasticity
- visual disturbances
- optic nerve atrophy – seen in around 25% of patients, often asymptomatic
- abnormalities of eye movements e.g. - square wave jerks; abnormalities of saccades, pursuit, fixation
- dysarthria
- present in more than 90% of individuals
- is an early sign
- hearing loss
- found in 8% to 13% of individuals
- dysphagia
- is common and present in around 92% of individuals with FRDA
- cognition
- cognition is generally not affected
- there can be impairment in verbal fluency, visuoconstructive and visuoperceptual capacity, and motor and mental reaction times
- non neurological features
- cardiac complications
- hypertrophic cardiomyopathy
- abnormal electrocardiogram
- diabetes mellitus
- skeletal abnormalities
- scoliosis
- foot abnormalities - pes cavus, talipes equinovarus
- sleep disordered breathing and sleep apnoea
- urinary frequency and urgency (1,2,3)
Atypical presentation is seen in 25% of patients with FRDA e.g. -
- late-onset FRDA (LOFA) and very late-onset FRDA (VLOFA)
- onset is later than age 25 years
- in LOFA, the age of onset is 26-39 years while in VLOFA, the age of onset is over 40 years
- FRDA with retained reflexes (FARR)
- FRDA in Acadian
- have a later age of onset and of wheelchair confinement, and a much lower incidence of cardiomyopathy (1,2,3)
Reference:
- (1) Bidichandani SI, Delatycki MB. Friedreich Ataxia. 1998 Dec 18 [Updated 2014 Jul 24]
- (2) Delatycki MB, Corben LA. Clinical Features of Friedreich Ataxia. Journal of child neurology. 2012;27(9):1133-1137
- (3) Parkinson MH et al. Clinical features of Friedreich's ataxia: classical and atypical phenotypes. J Neurochem. 2013;126 Suppl 1:103-17