Physical examination in a psychiatric patient Flashcards

(240 cards)

1
Q

Sign associated with neurosyphilis and diabetes

A

Argyll-Robertson pupil

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2
Q

Bilaterally small pupils which accommodate but do not react to bright light

A

Argyll-Robertson pupil

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3
Q

Sign where there are multiple surgical scars due to factitious disorder

A

Checker-board abdomen

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4
Q

Drug intoxication associated with constricted pupils

A

Opiates

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5
Q

Conditions associated with dilated pupils

A

Stimulant abuse
Anxiety
Opiate withdrawal

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6
Q

Eye sign associated with Wilson’s Disease

A

Kayser Fleischer ring

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7
Q

Neck sign associated with thyroid disease or rarely with lithium use

A

Goitre

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8
Q

Medical causes of gynaecomastia

A
Hyperprolactinaemia
Cirrhosis
Normal male puberty
Hypogonadism
Tumours including adrenal or testicular
Renal failure
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9
Q

Medication associated causes of gynaecomastia

A
Oestrogen containing drugs e.g. goserelin
Spironolactone
Finasteride
Ketoconazole
Methadone
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10
Q

Recreational drugs causing gynaecomastia

A

Marijuana
Amphetamines
Heroin

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11
Q

Body hair seen in anorexia nervosa

A

Lanugo

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12
Q

Disease causing lemon stick appearance

A

Cushing’s syndrome

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13
Q

Eye signs seen in hyperthyroidism

A

Exophthalmos
Lid retraction
Lid lag
Orbital fat prolapse

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14
Q

Disease classically associated with a mask-like face

A

Parkinson’s disease

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15
Q

Diseases associated with parotid swelling

A

Bulimia nervosa

Mumps

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16
Q

Sign seen in bulimia nervosa where there are callouses at the knuckles

A

Russell’s sign

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17
Q

Medication causing Sialorrhoea (hypersalivation)

A

Clozapine

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18
Q

Signs in infective endocarditis

A

Splinter haemorrhages
Osler nodes
Janeway lesions

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19
Q

Tender, red, raised lumps typically found on the fingers and toes in infective endocarditis

A

Osler nodes

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20
Q

Non-tender red lesions seen on the palms and soles of the feet in infective endocarditis

A

Janeway lesions

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21
Q

More common side for a unilateral paraesthesia caused by hyperventilation

A

Left

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22
Q

Usual distribution for paraesthesia caused by hyperventilation in a panic attack

A

Bilateral, upper limbs

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23
Q

Minor physical anomaly associated with developmental disorders where there is a skin tag in front of the ear

A

Preauricular skin tag

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24
Q

Syndrome occurring where there are lip pits and cleft lip/palate

A

Van der Woude syndrome

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25
Minor physical anomaly associated with developmental disorders where there are small white/grey spots in a ring around the pupil
Brushfield spots
26
Cranial nerve number I
Olfactory
27
Cranial nerve number II
Optic
28
Cranial nerve number III
Occulomotor
29
Cranial nerve number IV
Trochlear
30
Cranial nerve number V
Trigeminal
31
Cranial nerve number VI
Abducens
32
Cranial nerve number VII
Facial
33
Cranial nerve number VIII
Vestibulocochlear
34
Cranial nerve number IX
Glossopharyngeal
35
Cranial nerve number X
Vagus
36
Cranial nerve number XI
Accessory
37
Cranial nerve number XII
Hypoglossal
38
Main clinical examination technique for the olfactory nerve
Check sense of smell
39
Main clinical examination technique for the optic nerve
Visual acuity using Snellen charts Colour sight using Ishihara charts Visual fields Pupillary reflexes
40
Main clinical examination technique for the oculomotor nerve
Eye movements - elevation, adduction, depression in abduction Eyelid elevation Pupillary reflex
41
Main clinical examination technique for the oculomotor nerve
Eye movements - elevation, adduction, depression in abduction Eyelid elevation Pupillary reflex
42
Eye abnormality seen with a third cranial nerve lesion
Down and out
43
Main clinical examination technique for the trochlear nerve
Eye movements - depression in inversion
44
Eye abnormality seen in a fourth cranial nerve lesion
Upwards
45
Main clinical examination technique for the facial nerve
Facial movement | Taste for front 2/3 of the tongue
46
Main clinical examination technique for the trigeminal nerve
Sensation to the face | Chewing
47
Three branches of the trigeminal nerve
Ophthalmic Maxillary Mandibular
48
Main clinical examination technique for the abducens nerve
Eye movements - abduction
49
Eye abnormality seen in a sixth cranial nerve lesion
Eye turned inwards
50
Main clinical examination technique for the vestibulocochlear nerve
Balance - Romberg test | Hearing - Rinne/Weber tests
51
Main clinical examination technique for the glossopharyngeal nerve
Taste to the back 1/3 of the tongue | Sensation to the soft palate
52
Main clinical examination technique for the vagus nerve
Cough | Vocal cord movements
53
Main clinical examination technique for the accessory cranial nerve
Head turning | Shoulder shrugging
54
Main clinical examination technique for the hypoglossal cranial nerve
Tongue movements
55
Cranial nerve test where a vibrating tuning fork is held against the forehead in the middle of the face
Weber test
56
Cranial nerve test where a vibrating tuning fork is held at the mastoid bone, and then in front of the ear
Rinne test
57
Weber test result in normal hearing
Sound heard equally loudly bilaterally
58
Weber test result in conductive hearing loss
Sound louder in the abnormal ear
59
Weber test result in sensorineural hearing loss
Sound louder in the normal ear
60
Positive (normal) Rinne hearing test
Sound continues when the fork is moved from the bone to the air
61
Negative (abnormal) Rinne test
Sound does not continue when the tuning fork is moved from the mastoid to the air
62
Type of hearing loss associated with an abnormal Rinne test
Conductive hearing loss
63
Direction in which patients with poor vestibular function fall in a Romberg's test
Forwards to the side of the poor vestibular function
64
Testing for poor vestibular function in which cold or warm water is poured into an ear to elicit nystagmus
Caloric testing
65
Normal results in caloric testing in unilateral poor vestibular function
Cold water - nystagmus to the opposite side | Warm water - nystagmus to the same side
66
Test used to elicit ataxia
Heel toe walking
67
Cerebellar signs
``` Ataxia Hypotonia Intention tremor Past pointing Dysdiadokokinesis Dysarthria ```
68
Sign of meningism where flexion of the neck causes flexion of the knees and hips
Brudzinski sign
69
Sign of meningism where there is spasm if the knee is extended while the hip is flexed
Kernig sign
70
Sign suggestive of lower lumber nerve root irritation where the passive flexing of the hip while in the supine position causes pain
Straight-leg raising sign/Lasègue sign
71
Sign suggestive of upper lumbar nerve root irritation where there is pain on the passive hyper-extension of the hip while in the prone position
Reverse straight leg raise sign
72
Neurological signs which do not point to a lesion in a specific area
Soft neurological signs
73
Neurological sign where there are small quivering of the muscles
Fasciculations
74
Neurological sign where there are brief, jerky movements of the wrists on holding the arms out with the palms facing outwards
Asterixis
75
Slow, writhing spasms along the long axis of the limbs or the whole body
Athetosis
76
Semi-purposeful movements of the limbs affecting multiple joints; more peripheral than central
Chorea
77
Violent flinging movements of half of the body
Hemiballismus
78
Area of brain generally affected when primitive reflexes are seen in an adult
Diffuse cerebral damage, particularly in the frontal lobes
79
Primitive reflex where the arms jerk out and the head and legs extend on a sudden change of position
Moro reflex
80
Primitive reflex where the baby's head is turned to one side, and the arm on the side the head is turned straightens while the other arm bends at the elbow
Asymmetrical tonic neck reflex
81
Normal abdominal reflex
A line is drawn away from the umbilicus along a diagonal line, and the umbilicus is drawn towards the direction the line is drawn
82
Normal cremasteric reflex
Scratching the medial thigh in males causes elevation of the ipsilateral testis
83
Normal plantar reflex
Plantar flexion of the great toe on drawling a line up the sole of the foot
84
Positive Babinski sign
Dorsiflexion of the great toe on drawing a line up the sole of the foot
85
Spinal root of the biceps reflex
C5, C6
86
Spinal root of the brachioradialis reflex
C6
87
Spinal root of the triceps reflex
C7
88
Spinal root of the patellar reflex
L2-4
89
Spinal root of the Achilles reflex
S4
90
Lesions causing exaggerated tendon reflexes
UMN lesions
91
Lesions causing lack of tendon reflexes
LMN reflexes
92
Condition associated with frontal baldness
Myotonic dystrophy
93
Condition associated with ash leaf spots
Tuberous sclerosis
94
Condition associated with moles and dimples along the spine
Spina bifida occulta
95
Condition associated with Coast of Maine hyperpigmented skin lesions
McCune-Albright syndrome
96
Conditions associated with Café-au-lait spots
Neurofibromatosis, tuberous sclerosis
97
Condition associated with axillary freckling
Neurofibromatosis
98
Type of dysarthria characterised by a strained and hoarse voice with hypernasality, often with swallowing and drooling difficulties
Spastic dysarthria
99
Type of dysarthria characterised by a small tongue
Hypotonic dysarthria
100
Type of dysarthria characterised by loudness, tremor and irregularity
Ataxic dysarthria
101
Lesions associated with spastic dysarthria
UMN lesions
102
Lesions associated with hypotonic dysarthria
LMN lesions
103
Lesions associated with ataxic dysarthria
Cerebellar lesions
104
Type of dysarthria characterised by a quiet, breathy, monotone voice
Hypokinetic dysarthria
105
Type of dysarthria characterised by strained hoarseness and speech arrests
Hyperkinetic dysarthria
106
Lesions associated with hyperkinetic dysarthria
Basal ganglia lesions
107
Type of dysarthria characterised by sudden loss of voice, normal vocal cord movement and normal examination
Hysterical aphonia
108
Type of gait characterised by a paralysed leg which appears longer due to an extended knee, associated with a clenched hand on the ipsilateral side
Hemiparetic gait
109
Condition associated with a hemiparetic gait
Stroke
110
Type of gait characterised by a staggering, wide based gait
Ataxic gait
111
Area of lesion associated with an ataxic gait
Cerebellar
112
Type of gait characterised by very short steps
Shuffling gait
113
Type of gait characterised by progressively shorter steps due to acceleration while walking
Festinating gait
114
Condition associated with festinating gait
Parkinson's disease
115
Type of gait characterised by exaggerated steps, as if climbing stairs while walking on the flat
High stepping gait/neuropathic gait/equine gait
116
Condition associated with a high stepping gait
Chronic peripheral neuropathies
117
Type of gait characterised by a broad base, and the dropping of the pelvis on the side of the leg being raised, leading to a compensatory body swing forward
Waddling gait
118
Conditions associated with waddling gait
Proximal myopathy Congenital hip dislocation Pregnancy at near term
119
Type of gait characterised by over adduction and rigidity in the legs, causing the knees to rub together, as well as plantar flexion of the ankle causing forced tip toe walking
Scissoring gait
120
Condition associated with a scissoring gait
Spastic paraplegia
121
Type of gait characterised by the inability to lift the feet off the floor
Magnetic gait
122
Condition associated with magnetic gait
Normal pressure hydrocephalus
123
Conditions associated with absent ankle jerks and upgoing plantars
Subacute combined degeneration of the cord Neurosyphilis Friedrich's ataxia
124
Term for pupillary asymmetry
Anisocoria
125
Term for the denial of illness
Anosognosia
126
Lesion associated with anosognosia
Right frontoparietal lesion
127
Sign characterised by the upward deviation of the umbilicus when an attempt is made to sit up from the supine position due to lower abdominal paralysis
Beevor sign
128
Condition characterised by ipsilateral spastic paralysis and loss of position sense below the level of the lesion, hyperreflexia, and contralateral loss of pain and temperature sensation
Brown Sequard syndrome
129
Electrolyte abnormality causing Chvostek sign
Hypocalcaemia
130
Electrolyte abnormality causing Trousseau's sign
Hypocalcaemia
131
Sign characterised by facial spasm on the ipsilateral side when the cheekbone is tapped
Chvostek sign
132
Sign characterised by carpal spasm when a blood pressure cuff is tightened
Trousseau sign
133
Sign to test for brainstem integrity in a comatose patient where the head is moved quickly from side to side while the eyes are held open
Doll's eye manoeuver
134
Sign elicited in the doll's eye manoeuver if the brainstem is intact
Both eyes deviate to the opposite side to the direction the head is being turned
135
Condition associated with high foot arches, kyphoscoliosis, cerebellar signs, impaired joint position, cardiomyopathy and optic atrophy
Friedrich's ataxia
136
Sign associated with Duchenne's muscular dystrophy, where someone attempts to stand up by climbing up their own legs with their arms
Gower sign
137
Condition associated with a dilated pupil that reacts poorly to light, and absent patellar and Achilles reflexes
Holmes-Adie syndrome
138
Signs of horner's syndrome
``` Ptosis Anhydrosis Miosis Enophthalmos Loss of ciliospinal reflex ```
139
Tumour causing horner's syndrome
Pancoast tumour
140
Sign where the abnormal pupil dilates as a swinging light moves towards it from the normal side
Marcus Gunn pupil
141
Condition associated with a Marcus Gunn pupil
Afferent pupillary defect
142
Painful, asymmetric peripheral neuropathy with damage to at least two separate nerve areas
Mononeuritis multiplex
143
Causes of mononeuritis multiplex
``` Diabetes Vasculitis Amyloidosis Tumours Autoimmune disorders Paraneoplastic syndromes ```
144
Sign associated with chorea where someone cannot sustain a grip
Milkmaid's grip
145
Sign characterised by continued blinking with repeated glabellar taps (normally there is extinction of the reflex)
Myerson's sign
146
Condition associated with Myerson's sign
Parkinson's disease
147
Triad of optic neuritis
Loss of vision Eye pain Dyschromatopsia (decrease in the perception of colours)
148
Heat or exercise induced vision loss
Uhthoff sign
149
Sign characterised by an unsteady tongue when it is protruded out of the mouth, associated with chorea
Trombone tongue
150
Signs associated with an UMN lesion
Rigidity Hypertonia Hyperreflexia Mild atrophy from disuse
151
Signs associated with a LMN lesion
Atonia or hypotonia Loss of tendon reflexes Atrophy Fasciculations
152
Lesion causing a bulbar palsy
LMN lesion of cranial nerves IX - XII
153
Lesion causing a pseudobulbar palsy
Bilateral UMN lesions of the lower cranial nerves
154
Signs of a bulbar palsy
Wasted, fasciculating tongue Nasal speech Lack of jaw jerk Lack of gag reflex
155
Signs of a pseudobulbar palsy
Stiff tongue Donald-duck speech Exaggerated jaw jerk Emotional lability
156
Causes of a bulbar palsy
``` MND Polio Botulism Myasthenia Gravis Muscular dystrophy ```
157
Causes of a pseudobulbar palsy
MND MS Multi-infarct dementia Severe head injury
158
Area of brain lesion suggested by anomic dysphasia
Dominant temporo-parietal lesion
159
Failure to recognise an object despite normal visual input
Visual agnosia
160
First sign to improve when thiamine is given to a patient with Wernicke's encephalopathy
Ophthalmoplegia
161
Area of brain lesion suggested by poor visuospatial ability
Parietal lobe
162
Inability to read
Alexia
163
Area of brain lesion suggested in alexia without agraphia
Posterior cerebral territory (usually dominant)
164
Test used to identify patients with conversion disorder, where the patient is unable to lift their affect limb, but when lifting their unaffected limb against resistance is able to push down with their affected limb
Hoover's test
165
Area of brain lesion suggested by poor categorisation
Frontal lobe
166
Area of brain lesion suggested by poor error correction
Frontal lobe
167
Area of brain lesion suggested by a spastic hemiparesis
Contralateral frontal lobe
168
Hemisphere of brain lesion suggested by constructional apraxia
Right
169
Signs seen in a senile pupil
Sluggish light and accommodation reflex
170
Reductions in cognitive abilities seen in healthy aging
Motor speed Visuospatial skills Attention span New learning ability
171
Most common type of tremor
Benign essential tremor
172
Type of tremor which can be improved by alcohol and beta blockers
Benign essential tremor
173
Type of tremor which is not associated with pathology, which mostly affects the hands and which slowly progresses
Benign essential tremor
174
Type of tremor described as a 'pill-rolling tremor'
Parkinsonian
175
Type of tremor which is slow and coarse, and gets worse with intentional movement
Cerebellar/intention tremor
176
Type of tremor which is variable and improves with distraction
Psychogenic tremor
177
Type of tremor which is present in all normal people when maintaining a posture
Physiologic
178
Most coarse type of tremor
Cerebellar/intention tremor
179
Finest type of tremor
Physiologic
180
Features common in non-epileptic seizures compared to seizures
``` Longer duration Gradual onset and fluctuating course Eyes closed Safe fall Recall of the event ```
181
Features common in epileptic seizures compared to non-epileptic seizures
``` Sudden onset Incontinence (can occur in non-epileptic seizures too) Automatisms Biting of tongue or inside of mouth Amnesia for the event ```
182
Sustained muscle contractions which cause twisting movements or the maintenance of abnormal postures
Dystonia
183
Sudden involuntary (and not suppressible) jerks of a muscle or group of muscles
Myoclonus
184
Loss or absence of voluntary muscle movements
Akinesia
185
Slowness of movement seen in Parkinson's disease
Bradykinesia
186
Subjective feeling of inner restlessness
Akathesia
187
General term referring to problems with voluntary movements, or the presence of involuntary movements
Dyskinesia
188
Triad of features present in Parkinsonism
Tremor Rigidity Bradykinesia
189
Involuntary but somewhat suppressible stereotyped motor movement or vocalisation
Tic
190
Involuntary, rhythmic, alternating movement of one or more body parts
Tremor
191
Condition in which psychogenic polydipsia most commonly occurs
Schizophrenia
192
Features of sleep associated with typical depression
``` Decreased total sleep time Early morning wakening Prolonged sleep onset latency Increased wakening through the night Increased REM time Decreased slow wave sleep ```
193
Most typical sleep effect of depression
Early morning wakening
194
Dilation effect of mydriatic agents on Argyll Robertson pupils
Poor
195
Sign seen in Wilson's disease where there is a greenish central disc in the eye with spoke like yellow radiations
Sunflower cataract
196
Test used to investigate the cause of ataxia
Romberg test
197
Physical findings in hypothyroidism
``` Hair loss Bradycardia Periorbital puffiness Dry skin Coarse, brittle hair Myxoedema Hyporeflexia Tremor ```
198
Findings in hyperthyroidism
Hair loss Tachycardia Tremor Brisk reflexes
199
Test used during testing of visual fields where the patient's visual field is compared with the examiner's
Confrontation
200
Clinical features of acute cocaine intoxication
``` Increased temperature Labile BP and tachycardia Behavioural changes - euphoria, anxiety, agitation, paranoia Teeth grinding Dry mouth Dilated pupils ```
201
Clinical features of cocaine overdose
``` As for intoxication Rigidity and myoclonus Seizures Arrhythmias and ACS Hyperthermia induced rhabdomyolysis, renal failure or cerebral oedema ```
202
Clinical features of cocaine withdrawal
``` Vivid and unpleasant dreams Hypersomnia or insomnia Increased desire for sleep Irritability and anxiety Increased appetite Cravings ```
203
Clinical features of opiate overdose
Decreased level of consciousness Pinprick pupils Reduced respiratory rate
204
Clinical features of opiate withdrawal
``` Nausea, vomiting, diarrhoea Abdominal cramps Restless legs and muscle aches Anxiety Yawning Piloerection Coryzal symptoms and eye watering Pupillary dilation Tachycardia, hypertension ```
205
Clinical features of benzodiazepine overdose
Sleepiness Slurred speech Impaired balance and motor function Diplopia Paradoxical agitation, anxiety, hallucinations In severe cases coma, respiratory depression, hypotension, hypothermia, bradycardia
206
Clinical features of benzodiazepine withdrawal
``` Multiple features including: Anxiety, irritability and panic attacks Confusion Insomnia Weight loss Diarrhoea, nausea and retching Muscle twitching Photophobia Dilated pupils Tachycardia ```
207
Clinical features of cannabis intoxication
``` Euphoria Altered sense of time and mind Poor concentration and short term memory Increased appetite Anxiety, hallucinations, paranoia, psychosis Red eyes and sometimes dilated pupils ```
208
Clinical features of cannabis withdrawal
``` Irritability Anxiety Insomnia Decreased appetite Low mood Abdominal pain Tremors Sweating Headache Fever ```
209
Clinical features of alcohol withdrawal
``` Tremor Insomnia Agitation Seizures Hallucinations Sweating Disorientation Autonomic instability Nausea and vomiting ```
210
Clinical features of ecstasy intoxication
``` Euphoria Dilated pupils Dehydration Hyperthermia Tachycardia and hypertension Nausea, vomiting and diarrhoea Clenching of jaw ```
211
Clinical features of ecstasy overdose
``` Labile BP Hyperreflexia Confusion, paranoia, agitation Muscle rigidity Hyperpyrexia ```
212
Sign where the pupils constrict and then widely dilate due to raised intracranial pressure
Hutchinson pupil
213
Gait seen in hip dysplasia or other strucural abnormalities
Pigeon gait
214
Gait seen in Friedreich's ataxia
Stomping gait
215
Clinical features of amphetamine intoxication
``` Tachycardia or bradycardia Labile BP Pupillary dilation Sweating or chills Nausea and vomiting Euphoria, anxiety, paranoia (in amphetamine induced psychosis) ```
216
Clinical features of amphetamine withdrawal
``` Cravings Low mood Increased appetite Increased or decreased movement Change in sleep patterns Lucid dreams ```
217
Type of lesion which causes pronator drift
Upper motor neurone lesion
218
Type of gait characterised by a long swing phase and short stance phase on one side
Antalgic gait
219
Symptom associated with an antalgic gait
Pain on weight bearing
220
Percentage of patients with autism who also have macrocephaly
20%
221
Features of a lower motor neurone lesion
``` Weakness Marked atrophy Fasciculations Decreased tone Decreased reflexes ```
222
Features of an upper motor neuron lesion
``` Weakness Mild atrophy only Increased tone Increased reflexes Upgoing plantars (Babinski) Clonus ```
223
Weakness of one side of the body
Hemiparesis
224
Paralysis of one side of the body
Hemiplegia
225
Apraxia where there is an inability to plan and complete motor tasks, and to convert an idea into action. May have retained ability to complete the task if not consciously thinking about it or may do the wrong thing e.g. try to brush their hair with a razor.
Ideomotor apraxia
226
Type of apraxia where someone is unable to brush their teeth when asked to. If handed a toothbrush with toothpaste on they may try to perform the wrong action.
Ideomotor apraxia
227
Type of apraxia where there is an inability to conceptualise and complete multistep tasks. May complete tasks in the wrong order e.g. putting on shoes before socks
Ideational apraxia
228
Type of apraxia where someone is unable to make a slice of buttered toast, even though they can repeat each single step when shown by others
Ideational apraxia
229
Type of apraxia where there is an inability to make fine or delicate movements
Limb kinetic apraxia
230
Type of apraxia where there is an inability to copy a picture or combine parts of something to form something whole
Constructional apraxia
231
Type of apraxia where there is an inability to control eye movements properly
Oculomotor apraxia
232
Psychiatric condition where there is a deficit in smooth eye tracking
Schizophrenia
233
Percentage of patients with Wernicke's who have the classic triad of symptoms
10%
234
Physical signs that can point towards a metabolic or toxic cause of altered mental state
Asterixis Tremor Myoclonic jerks
235
Eye sign which is pathognomic of multiple sclerosis
Bilateral internuclear ophthalmoplegia
236
Features of internuclear ophthalmoplegia
Impaired adduction | Abducting nystagmus
237
Length of time post traumatic amnesia should last with a mild head injury
Less than one hour
238
Length of time post traumatic amnesia should last with a moderate head injury
1 hour to 24 hours
239
Length of time post traumatic amnesia should last with a severe head injury
More than 24 hours
240
Level of lesion associated with pronator drift
UMN lesion