Peripheral Polyneuropathy Flashcards
3 categories of inherited polyneuropathies
Hereditary Motor and Sensory Neuropathy
Hereditary Sensory and Autonomic Neuropathy
Hereditary Motor Neuropathy
Most commonly inherited polyneuropathy
Hereditary motor and sensory neuropathy, AKA Charcot-Marie Tooth Disease
Recurrent short term episodes of motor and sensory mononeuropathies due to nerves being sensitive to pressure
Hereditary neuropathy with liability to pressure palsy (HNPP)
HMSN is similar to what else in terms of same gene mutation
HNPP (hereditary neuropathy with liability to pressure palsy)
Sensory loss along with thermal day’s regulation, bladder dysfunction and cognitive deficits
Hereditary sensory and autonomic neuropathy
Progressive weakness and atrophy of UE and LE
Hereditary motor neuropathy
Most common acquired polyneuropathy
Diabetes mellitus
Typical distribution of symptoms of acquired polyneuropathy
Symptoms are distal and progresses proximally
Multifocal motor neuropathy
Demyelination vs. axonal
Motor vs. sensory
Demyelinating
Motor
HMSN I, II, III, IV
Demyelination vs. axonal
Motor vs. sensory
I, III, IV = demyelinating, sensorimotor
II = axonal, motor > sensory
AIDP and CIDP
Demyelination vs. axonal
Motor vs. sensory
AIDP = Demyelinating or axonal, motor > sensory CIDP = demyelinating, motor > sensory
Diabetic neuropathy
Demyelination vs. axonal
Motor vs. sensory
Demyelination and axonal loss
Sensorimotor
Lead toxicity
Demyelination vs. axonal
Motor vs. sensory
Axonal loss
Motor > sensory
B12 deficiency
Demyelination vs. axonal
Motor vs. sensory
Axonal loss
Sensorimotor
Friedrich’s ataxia
Demyelination vs. axonal
Motor vs. sensory
Axonal
Sensory