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Congenital myopathy:
featuresDREAMS:
Dominantly inherited, mostly Balint's syndromeSOOT:
Reflexes decreased Simultagnosia
Enzymes normal Optic ataxia Stroke: basic work up The 3
Apathetic floppy baby Ocular apraxia P's:
Milestones delayed Tunnel vision Pump
Pipes
Plasma
Neurofibromatosis: Stroke: young patient's likely
diagnostic causes 7 C's:
criteriaROLANDO: Cocaine Head trauma: rapid neuro
Relative (1st degree) Consanguinity [familial such as exam · 12 P's:
Osseous fibromas neurofibromatosis and von Psychological (mental) status
Lisch nodules in eyes Hippel-Lindau] Pupils: size, symmetry,
Axillary freckling Cancer reaction
Neurofibromas Cardiogenic embol Paired ocular movememts
Dime size cafe au lait spots hyperCoagulation Papilloedema
Optic gliomas CNS infection [eg: HIV Pressure (BP, increased ICP)
conditions] Pulse and rate
Congenital arterial lesion Paralysis, Paresis
Pyramidal signs
Pin prick sensory response
Pee (incontinent)
Proximal myopathy: Patellar relex (and others)
differentialPEACH PODS: Ptosis
Polymyositis Encephalitis: · Reevaluate patient every 8
Endocrine: hyper, differentialHE'S LATIN hrs.
hypothyroidism, Cushing's AMERICAN:
syndrome, acromegaly Herpesviridae
Alcohol Enteroviridae (esp. Polio)
Carcinoma Slow viruses (esp. JC, prions)
HIV infection Syphilis
Periodic hypokalemic paralysis
Legionella/ Lyme disease/ Neurofibromatosis:
Osteomalacia Lymphocytic diagnositic criteria (type-
Drugs: steroids, statins meningoencephalitis 1)CAFE
Sarcoidosis Aspergillus SPOT:
Toxoplasmosis Cafe-au-lait spots
Intracranial pressure Axillary, inguinal freckling
Neisseria meningitidis Fibroma
Arboviridae Eye: lisch nodules
Measles/ Mumps/ Skeletal (bowing leg, etc)
Dementia: reversible Mycobacterium tuberculosis/ Pedigree/ Positive family
dementia causesDEMENTIA: Mucor history
Drugs/ Depression E. coli Optic Tumor (glioma)
Elderly Rabies/ Rubella
Multi-infarct/ Medication Idiopathic
Environmental Cryptococcus/ Candida
Nutritional Abscess
Toxins Neoplasm/ Neurocysticercosis
Ischemia · Neurocysticercosis should be Pupillary dilatation
Alcohol assumed with recent Latin (persistent): causes3AM:
American immigrant 3rd nerve palsy
patient unless proven Anti-muscarinic eye drops (eg
otherwise. to facilitate fundoscopy)
Myotonic pupil (Holmes Adie
pupil): most commonly in
young women, with
absent/delayed reaction to light Tabo paresis Injury
and convergence, and of no Syringobulbia Tumor
pathological Spin (benign positional vertigo)
significance.
Peripheral neuropathies:
differentialDANG Ramsay-Hunt syndrome:
Ocular bobbing vs. dipping THERAPIST: cause and common feature
"Breakfast is fast, Diabetes "Ramsay
Dinner is slow, both go down": Amyloid Hunt":
Bobbing is fast. Nutritional (eg B12 deficiency) · Etiology:
Dipping is slow. Guillain-Barre Reactivated
In both, the initial movement is Toxic (eg amiodarone) Herpes zoster
down. Heriditary · Complication:
Endocrine Reduced
Recurring (10% of G-B) Hearing
Alcohol
Pb (lead)
Idiopathic
Huntington's: chromosome, Sarcoid
involvementHUNT 4 DATE: Thyroid
HUNTington's on chromosome Stroke risk factorsHEADS:
4, with cauDATE nucleus Hypertension/ Hyperlipidemia
involvement. Elderly
Atrial fib
Diabetes mellitus/ Drugs
Dementia: some common (cocaine)
causesDEMENTIA: Smoking/ Sex (male)
Diabetes
Pin-point pupil causesPin- Ethanol
Point Pupils Medication
are due to oPioids and Pontine Environmental (eg CO
Pathology poisoning)
Nutritional Multiple sclerosis (MS):
Trauma epidemiologyMS is a
Infection feminine title (Ms.) and is
Alzheimer's female predominant.