Block 6 W4 Flashcards
What are the 4 aspects of learning disabilities?
- significant impairment in intelligence - IQ.
- significant impairment in adaptive behaviour - reading, writing, numeracy.
- Significant impairment in social functioning - varies with diagnosis.
- onset during developmental period (<18 years).
Describe the Stanford-Binet scale for measuring intelligence.
Guages intelligence through 5 factors of cognitive ability:
- fluid reasoning
- knowledge
- quantitative reasoning
- visual-spatial processing
- working memory
How is IQ measured?
IQ = (mental age/chronological age) x 100
What is the Wechsler adult intelligence scale (WAIS)?
Stanford Binet wasn’t appropriate for adults as it relied too heavily on language ability.
Includes verbal and performance sub scales.
Describe the normal distribution of IQ.
LD - if IQ less than 70 (2SD below the mean of 100)
50-70 -> mild LD
35-49 -> moderate
20-34 -> increased sensory and motor deficits, 50% have epilepsy.
<20 -> profound, developmental level 12 months.
How does trauma cause LD?
Related to forceps delivery or ventouse delivery -> could damage the brain.
How does toxin cause LD?
Foetal alcohol syndrome:
- underdeveloped jaw
- smooth philtrum
- low nasal bridge
- small head
- flat midface
Describe the genetics of tuberous sclerosis.
Autosomal dominant disorder
Affects genes that contribute to production of hamartin and tuberin (TSC 1 - Ch9, TSC 2 - Ch16) -> responsible for halting growth of tumours.
Causes growth of hamartomas across the body - brain, skin, kidneys, heart.
Describe the signs of tuberous sclerosis.
Adenoma sebaceoum are tumours that are vascular and fibrous in origin and found on cheeks or within folds at the side of mouth and nose.
Areas of macular hypo-pigmentation occurs in ovoid or leaf-shapes.
Sections of cerebral cortex show tuber life growths on brain, which calcify and become sclerotic.
Thus, 50% have LD.
How does genetics contribute to LD?
Down’s syndrome - 95% caused by trisomy Ch21
People with DS living longer now.
45% over 45 develop Alzheimer’s -> cerebral atrophy.
Describe the metabolic causes of LD.
Autosomal recessive gene Phenylketonuria - 1/10,000 births -> absence of phenylalanine hydroxylase -> build up of phenylalanine: - microcephaly - epilepsy - over activity - autism - albinism - musty odor People with PKU can't produce tyrosine, AA, involved in melanin production -> fair skinned and blue eyes.
Describe the Guthrie test.
Primary diagnostic test for PKU - measurement of phenylalanine levels in drop of blood taken from heel of a newborns foot.
Screening procedure
PKU confirmed by appearance of bacteria growing around high conc. of phenylalanine in blood spot.
Normal development occurs with low phenylalanine diet and drugs.
What are the major infections that causes LD?
T - O - toxoplasmosis R - rubella C - cytomegalovirus and congenital syphilis H - herpes
How does the foetus contract toxoplasmosis?
Through placental connection with infected mother.
Mother infected by improper handling of cat litter or contaminated meat.
Describe the Toxoplasmosis gondii.
Protozoa
Found in undercooked meat, raw meat and cat faeces.
25-50% of worlds population is infected and around 1% in UK catch toxoplasmosis/year.
Causes flu-like symptoms - affects babies/foetuses, immune deficient people.
Describe cerebral infections.
Meningitis and encephalitis -> rare complication of common infections. Rate decreased due to MMR vaccine.
Herpes simplex virus - most common cause.
Describe the morbidity and mortality of LD patients.
- Significant physical health needs - 74% needed specialist care.
- Life expectancy markedly reduced - directly proportional to level of disability.
- Death by indifference -> neglected within healthcare, delayed diagnosis and treatment, institutional discrimination.
- Significant increased mental disorder compared to general population.
What services are available to LD patients?
GP, hospital, liaison nurse, community LD team, inpatient services.
Independent sector organisations e.g. Wilf Ward family trust and Mencap.
Define psychosis.
Fundamental and characteristic distortions of thinking and perception. Clear consciousness and intellectual capacity is usually maintained.
Describe the ICD-10 diagnostic requirement for schizophrenia.
1 syndrome or 2 symptoms for most of the time for at least 1 month.
Not manic or depressive episode or at least present before these.
Not attributable to organic brain disease.
Not attributable to alcohol or drug-related intoxication, dependence or withdrawal.
List the symptoms of schizophrenia.
- thought echo, insertion, withdrawal or thought broadcasting
- delusions of control, influence or passivity of thought, action or sensation
- delusional perceptions
- persistent delusions that are bizarre or impossible
- catatonic behaviour i.e. mutism, stupor, posturing
- disordered thought (derailment, incoherence, neologisms, irrelevance)
- hallucinatory voice in 3rd person, discussing, running commentary or coming from part of body
- negative symptoms
What are the 7As of negative symptoms?
Apathy (lack of interest) Avolition (lack of motivation) Anergia (lack of energy) Alogia (poverty of speech) Anhedonia Asociality (lack of social interaction) Affective flattenening (restricted range of emotions)
Describe the cognitive symptoms in schizophrenia.
Average IQ = 95 -> declines after 1st episode
Discrepancy in verbal/non-verbal IQ
Impaired attention
Over-inclusiveness, verbal redundancy
Describe Liddle’s 3 syndrome model.
- reality distortion - hallucinations, delusions
- disorganisation - thought disorder, inappropriate affect
- psychomotor poverty - poverty of speech, blunted affect
What are the structural findings of the brain in psychosis?
- increased ventricle volume
- decreased volume of cortex
- more neurones with less connections
- functional imaging shows patterning of activity that reflects symptoms:
- auditory hallucinations -> Broca’s area
- negative symptoms -> prefrontal cortex
- passivity -> cingulate gyrus
Explain the epidemiology of schizophrenia.
M=F Earlier peak onset in males (22 vs. 26) Incidence - 1-2/10,000 per year Lifetime prevalence - 1% Urban > rural (2-3x risk) Most common in SEC IV & V.
What are the prenatal risk factors of schizophrenia?
- premature birth
- unwanted pregnancy
- maternal influenza
- rubella
- malnutrition
- associated medical problems e.g. diabetes
What are the obstetrics and neonatal risk factors of schizophrenia?
- obstetrics complications
- low birth weight
- hypoxia
- association with structural brain abnormalities
What are the early childhood risk factors of schizophrenia?
- mixed handedness (crow)
- mixed hand and eye dominance (cannon)
- late milestones
What are the adult risk factors of schizophrenia?
- age
- gender effects
- urban vs. rural
- migrants risk is 4-6x greater in 2nd generation, declining in subsequent generations.
What are the late risk factors of schizophrenia?
Precipitants: - life events - substance abuse Cannabis - dose response effect, gene x environment. Low CBD:THC ratio worse. Amphetamines/cocaine/crack Hallucinogens
What is the dopamine hypothesis of psychosis?
Increased dopamine activity in striatal dopaminergic neurones -> psychosis.
Increased synaptic release and D2 receptor occupancy.
- acutely psychotic individuals -> have excessive striatal release of dopamine
- excessive dopamine release leads to aberrant assignment of salience to unimportant stimuli
- delusions may arise from attempts to explain this abnormal salience.