Sit to stand Stance walk to 6m. Part of foot landing Stride length foot clearancd Wide based more than shoulder or more than 12cm. In ataxia cerebellar or sensory or vestibular Arm swing Turning en bloc more than 3 steps Romberg to differentiate cerebellar and sensiry. Push and pull
Psp falls back Parkinson's falls forward.
Freq falls Neuro ataxia, post instability Parkinson, Parkinson's trap Cerebellar signs NPH bladder bowel dementia Multiinfarct vascular dementia. Ll Vestibular nystagmus tinnitus vertigo Non neuro e.g. msk
Examination inspection includes movement disorders involuntary movements. Tone is for movement disorders and corticospinal Reflexes and power is for corticospinal tract UMN and LMN Coord is for cerebellar Sensory loss is for pattern and modality. dermatomal distribution. Peripheral nerve aphenous, spn. Glove stocking. Pinprick is spinothalamic and small fibre. Proprioception is for dorsal column and large fibre. Sensory symptoms brain or peripheral nerve.
Wasting and fasciculatikns. Lmn and distribution. - quadriceps think of LMN l2 to lumbar plexus to femoral nerve . Or diffuse. Deformity foot drop, pes cavus in cmt, Charcot joint dm neuropathy ulcers - dm. Skin is indicates autonomic function.
Tone for umn Vs lmn
Reflex kj l3 4 femoral nerve. AJ diminished l5 S1 or peripheral neuropathy. plantar response Power. ankle dorsiflex l4 l5 common peroneal. Toe l5. ankle plantar flexion S1 tibial nerve sciatic nerve gastroc soleus.
Vibration sense do IPJ of toe. If cerebellar signs, proceed to finish e.g. head and truncal titubation, nystagmus, dyaarthia British constitutikn, dysmtetria (multi joint.) , dysdiadochokinesia ("faster and higher").
Vermis is nvolvemrnt is nystagmus and truncal. Hemispherical involves appendices. Flocculonodular lobe. Vertigo spinocerebellar pathway - Spinocerebellar ataxia.
unilateral means structural Bilateral means metabolic e.g. toxins
50yo m no PMH except mvp. Sudden onset unsteadiness and disorientation. No weakness njmbness. No slurring ,diplopia, dysphagia.
examine cranial nerves.
Inspect face for ptosis, Ptosis (Horner syndrome) + ataxia = lateral medullary syndrome ptosis is levator palpebrae superioris weakness myopathies. nmj (fatiguability), CN iii (DM or surgical) Midbrain (long tract signs)
multidirdctiibak nystagmus Decreaded sensation right side of face. Facial nerve
Palate sluggish
Complex ophthalmoplegia if it doesn't fit into one nerve
Parkinson's examine ul. Look at the face!! Test apraxia for cbgd i.e. cannot copy (cannot perform learned movement but no motor or sensory issue. Can also ask Hx brush teeth comb hair.)
episodic disorders rely on Hx Headache. Just need fundus Epilepsy long case - onset, frequency, type of seizures. How under control?
Hx and pe neuro signs Motor with objective weakness, ataxia, movement disorder including involuntary movements decreased increased or abnormal. Sensory radiculopathy neuropathy spinal cord or cns. Cortical - dementia etc. Cranial nerve deficits
Mg ocular ptosis diplopia. Bulbar symptoms. Proximal muscle. Resp diaphragm. Fatiguability, diurnal variation. Compare both sides for shoulder abduction.
Foot drop 50% cpn. ankle dorsiflexoon. Tib anterior. Deep peroneal common sciatic nerve sacral plexus. L4l5. Cpn also involves superficial peroneal nerve sensation and eversion Sciatic also involves tibial nerve i.e. plantar flexors and inversion. If cannot walk on toes means plantar weakness. Proximal sciatic nerve involves knee extensions Sacral plexus supplies hip abduction and extension L4 l5 - need to check sensation Corticospinal - spasticity.
Wrist drop 90% radial nerve ECU ecrlb. Radial nerve brachial plexus, posterior cord, posterior divisoons, c5 to c8
Pin only affects motor to thumb eip fingers, no sensory srn.
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