LPT Gondar Mental Health Group www.le.ac.uk Learning Disability or - - PowerPoint PPT Presentation

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LPT Gondar Mental Health Group www.le.ac.uk Learning Disability or - - PowerPoint PPT Presentation

Concept & Causes of Learning Disabilities LPT Gondar Mental Health Group www.le.ac.uk Learning Disability or Mental Retardation Important! Exam questions only from workbook The lecture names many conditions the aim of this is to


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Concept & Causes of Learning Disabilities

LPT Gondar Mental Health Group

www.le.ac.uk

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Learning Disability or Mental Retardation

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Important!

 Exam questions only from workbook  The lecture names many conditions the aim of

this is to increase your awareness of these disorders not for you to remember each one!

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Concepts - Learning Disability

 A general concept  Intellectual functioning & IQ  Mental Age  Epidemiological concept  Clinical - ICD 10 & DSM IV  Medico-legal concept

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Learning Disability General Concepts

 Affects ability to learn  Impairs cognition  Is only one attribute of people with LD  Is a serious disability  Are people first  Have hopes and dreams like everyone else  Face many obstacles  Often require considerable support

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Intellectual functioning

 A theoretical construct  A human trait distributed in a predictable

manner

 IQ =

Mental age X 100 Chronological age

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Mental Age

 Is defined as the developmental level acquired

by an individual

 Is an outdated way to classify and describe an

individual’s abilities

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Learning Disability Epidemiological Concept

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Learning Disability Clinical concept

 Six criteria (E. A. Doll, 1941)  social incompetence  due to mental subnormality  which has been developmentally arrested  which obtains at maturity  is of constitutional origin  is essentially incurable

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Learning Disability Clinical concept

 The definition specifies three criteria  significantly subaverage intelligence  impaired adaptive behaviour or functioning  origin during the developmental period

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ICD 10 Definition

 Mental Retardation is defined as a condition of arrested

  • r incomplete development of the mind, which is

characterised by impairment of skills manifested during the developmental period, which contribute to the overall level of intelligence, e.g. cognitive, language, motor and social abilities.

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ICD 10 Definition

 Sub average intellectual functioning  At least two limited areas of adaptive

functioning exist concurrently

 The disability occurred before the age of 18

years

 All three criteria need to be satisfied

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Mental Retardation Classification based on IQ < 70

 Mild MR:

IQ 50 – 70

 Moderate MR: IQ

35 – 49

 Severe MR:

IQ 20 – 34

 Profound MR:

IQ < 20

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Adaptive skill areas

 Communication  Self-care  Home living  Social skills  Community use  Self-direction  Health and safety  Functional academics  Leisure  Work

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Causes of Learning Disability

 Prenatal

  • 70%

 Perinatal

  • 9%

 Postnatal

  • 2%

 Familial/Cultural

  •  Unidentifiable
  • 19%
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Prenatal Causes

 Genetic disorders

 Chromosomal aberrations  Single gene mutations

 Autosomal dominant  Autosomal recessive  X linked disorders

 Microdeletions

 Congenital malformations  Exposure

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Prenatal causes – Genetic disorders

Chromosomal aberrations

Autosomal abnormalities Sex chromosomal abnormalities

Microdeletions Single gene mutations

Autosomal dominant disorders Autosomal recessive disorders X linked disorders

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Chromosomal aberrations

Abnormalities of autosomes Downs syndrome – Trisomy 21 Edwards syndrome – Trisomy 18 Pataus syndrome - Trisomy 13 Abnormalities of sex chromosomes Fragile X syndrome – fragile site on Xq27-28 Klinefelter’s syndrome – 47, XXY Turners syndrome – 45, XO

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Partial deletions & Microdeletions

Prader-Willi syndrome

  • microdeletion of paternal 15q

Williams syndrome

  • microdeletion of 17

Cri du chat syndrome

  • partial deletion of 5
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Autosomal dominant disorders

 Tuberous sclerosis (Epiloia)  Neurofibromatosis (von Recklinghausen’s

disease)

 Encephalofacial angiomatosis (Sturge – Weber

syndrome)

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X – linked disorders

 Fragile X syndrome  Lesch-Nyhan syndrome  Haemoglobin (HbH) disease with mental

retardation

 ATR-X syndrome (α – thalassaemia/mental

retardation syndrome)

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Prenatal causes - Congenital anomalies

 CNS malformations

 Neural tube defects

 Multiple malformations syndromes

 Cornelia de Lange syndrome

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Epidemiology of Genetic disorders

Genetic disorders/congenital anomalies apparent by age 25: 79 per 1000 livebirths

  • 1. Single gene (Mendelian) disorders

Incidence: 3.6/1000

  • a. Autosomal dominant

Incidence: 1.4/1000

  • b. Autosomal recessive

Incidence: 1.7/1000

c.

X-linked disorders Incidence: 0.5/1000

  • 2. Chromosome abnormalities

Incidence: 1.8/1000

  • 3. Multifactorial conditions (onset <25)

Incidence: 46.4/1000

  • 4. Conditions that appear genetic but precise mechanism unknown

Incidence: 1.2/1000

  • 5. Other congenital anomalies

Incidence: 26/1000

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Prenatal - Exposure

 Maternal infections  Congenital rubella (Rubella syndrome), HIV  Teratogens  Fetal alcohol syndrome  Toxaemia, placental insufficiency  Prematurity  Trauma  Iatrogenic  Radiation, Drugs  Severe malnutrition  IUGR

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Perinatal causes

 Infections  Delivery

 Anoxic brain damage

 Others

 Hyperbilirubinaemia

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Postnatal causes

 Infections

Encephalitis

 Metabolic

Hypoglycaemia

 Endocrine

Cretinism

 Cerebrovascular

Thrombo-embolism

 Toxins

Lead poisoning

 Trauma

Head injury

 Neoplasms

Meningioma, Cranipharyngioma

 Psychosocial factors Understimulation

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Clinical syndromes

 Downs syndrome  Fragile X syndrome  Tuberous sclerosis  Phenylketonuria  Cornelia de Lange syndrome  Edwards syndrome  Prader Willi syndrome  Angelman syndrome  Lesch Nyhan syndrome  Other inborn errors  amino acid metabolism  Fatty acid metabolism  Carbohydrate metabolism  Nucleic acid metabolism  Smith Magenis syndrome  Williams syndrome

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Downs syndrome

 Physical features

 Facies, somatotype, Congenital anomalies, Infantile spasms,

Hypothyrodism

 Psychiatric associations

 Dementia  Depression  Hyperactivity  Conduct disorder  Autism

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Phenyketonuria

 Physical features

 Blond hair, blue eyes, spasticity, epilepsy

 Psychiatric associations

 Autism  Hyperactivity  Epilepsy

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Management

 Assessment is key  Effective communication,  Treat any coexistent mental disorders-

psychosis, depression, anxiety

 Adapt environment to meet the needs of the

person

 Maintain quality of life as much as possible  Support the family

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Provided by The Leicester Gondar Link Collaborative Teaching Project

This work is licensed under a Creative Commons Attribution-NonCommercial- NoDerivs 3.0 Unported License.