Skip to main content
. 2021 Apr 7;35(6):e23772. doi: 10.1002/jcla.23772

TABLE 2.

Clinical features of family members carrying the NM_001256443:c.641dupC mutation

Feature Patient
a b c
Age, years 54 60 56
Age at onset 44 20 46
Spastic gait + Wheelchair from last 5 years +
Urinary urgency
Scoliosis +
Upper limbs
Weakness
Sensory loss
Lower limbs
Increased tone + + +
Hyperreflexia + + +
Weakness + + +
Extensor plantar response + + +
Sensory loss + + +
Decreased vibration sense + + +

(+), present; (−), absent.