Mental Retardation Disease

BASICS

DESCRIPTION

Mental retardation (MR) is a symptom with multiple etiologies including chromosomal abnormalities, genetic defects, intrauterine, perinatal, neonatal, and postnatal causes. Mental retardation refers to substantial limitations in present functioning. It is characterized by significantly subaverage intellectual functioning, existing concurrently with related limitations in two or more of the following applicable adaptive skills areas: communication, self-care, home living, social skills, community use, self-direction, health and safety, functional academics, leisure and work. Cognitive and adaptive behavior deficits are manifested before age 18.

  • Subgroups of mentally retarded:
    • Mild: IQ 55-69 (85%)
    • Moderate: IQ 40-54 (10%)
    • Severe: IQ 25-39 (5%)
    • Profound: IQ 0-24 (<1%)
  • System(s) affected: Nervous
  • Genetics:
    • Autosomes: Trisomies and rearrangements - approximately 1500 variations are all associated with MR
    • Sex chromosomes: 80 of 336 disorders cause MR
    • Autosomal dominant: 180 of 3,000 disorders cause MR
    • Autosomal recessive: 400 of 1,550 disorders cause MR
  • Incidence/Prevalence in USA: Incidence and prevalence are closely related to social, economic, and health conditions of the society. The general incidence of mental retardation in the United States has been estimated at 125,000 births per year by the American Association on Mental Retardation. This would correspond to approximately 3% of the population. The research on both incidence and prevalence of mental retardation in the US is exceedingly scant. A comprehensive Canadian study of the maritime Provinces found prevalences of 3.65 per 1000. Most professionals associated with the American Association on Mental Retardation accept a prevalence of 2.5% and they recognize that the prevalence varies with chronological age. Specifically, mildly retarded preschoolers are able to meet societies demands but are identified by the school system due to demands for cognitive processing. Conversely, once they leave the requirements of the educational system they may adapt to societies demands and the diagnosis need not apply.
  • Predominant age: By definition mental retardation occurs during the developmental period. Older adults who lose mental faculties are more accurately diagnosed as demented. Patients may present the MR after traumatic brain injury.
  • Predominant sex: Male > Female (1.5:1)
SIGNS AND SYMPTOMS
  • Profoundly and severely retarded children are frequently diagnosed at the time of birth or during the newborn period. Children with profound or severe retardation are more likely to have dysmorphic features.
  • Moderately retarded children may go undiagnosed until they fail to meet normal developmental milestones.
  • Mildly retarded children may go undiagnosed until well into the school years.
CAUSES
  • Chromosomal abnormalities
    • Autosomal abnormalities
    • Trisomy, e.g., Down syndrome
    • Translocations
    • Inversions
    • Duplications
    • Deletions, e.g., Prader-Willi
  • Sex chromosome abnormalities
    • Fragile X mutation
    • Turner syndrome
    • Klinefelter syndrome
    • Rett syndrome
    • Various multiple X and/or Y conditions
  • Autosomal dominant conditions
    • Neurocutaneous syndromes, e.g., neurofibromatosis, tuberous sclerosis
  • Autosomal recessive conditions
    • Amino acid metabolism, e.g., phenylketonuria, Maple syrup urine disease
    • Carbohydrate metabolism, e.g., galactosemia, fructosuria
    • Lipid metabolism
      • Tay-Sachs
      • Gaucher
      • Niemann-Pick, e.g., mucopolysaccharidosis
    • Purine metabolism, e.g., Lesch-Nyhan
    • Other, e.g., Wilson
  • Multifactorial and sporadic conditions
    • Cornelia de Lange syndrome
    • Spinal cord disorders (spina bifida, Arnold-Chiari malformation)
    • Disorders of brain and skull
    • Prenatal factors
    • Rh incompatibility
    • Maternal infections - all the TORCH viruses: rubella, toxoplasmosis, cytomegalic virus, and herpes simplex
    • Maternal diseases, e.g., diabetes mellitus, toxemia
    • Maternal substance abuse, e.g., alcohol use/abuse. Fetal alcohol syndrome is a leading environmental cause of mental retardation.
    • Prescription medications, such as Accutane or Dilantin
  • Perinatal factors
    • Prematurity
    • Postmaturity
    • Birth injuries
    • High risk mothers
  • Postnatal factors
    • Childhood diseases, e.g., meningitis, encephalitis, general inflammatory disease with high fever, hypothyroidism
    • Trauma, e.g., accidents, physical abuse, marked deprivation
    • Poisoning, e.g., lead, carbon monoxide, household products
RISK FACTORS

Risk factors for future offspring of the parent couple must be calculated based upon the specific etiology of related retarded individuals

DIAGNOSIS

LABORATORY
  • Specific studies are available for those patients with identifiable genetic disease entities
  • Chromosome studies
  • Metabolic screens
  • Amino acid
  • Sugar substrates
  • Molecular studies, e.g., DNA

Drugs that may alter lab results: N/A
Disorders that may alter lab results: N/A

PATHOLOGICAL FINDINGS

N/A

SPECIAL TESTS
  • Individually administered measure of intellectual abilities
    • Measure utilized depends upon the age of the patient
    • Birth through 42 months: Bayley's Scales of Infant Development
    • 2 years of age through adulthood:
    • Stanford Binet (form LM)
    • Stanford Binet (4th edition)
    • Wechsler Scales
    • Preschool children: WPPSI
    • School age: WISC-III
    • Adults:
    • WAIS-III
    • Adaptive behavior scale. All patients need a measure of adaptive behavior. The Vineland Adaptive Behavior Scales are widely utilized.
    • Other measures are available; however, these are the most widely recognized and utilized measures of individual ability and adaptive behavior
IMAGING

N/A

DIAGNOSTIC PROCEDURES

See Special tests

TREATMENT

APPROPRIATE HEALTH CARE
  • Some specialized care may be necessary based upon the etiology of the retardation
  • Care for the retarded is educational, not medical and should include early intervention
GENERAL MEASURES

N/A

SURGICAL MEASURES

N/A

ACTIVITY

Full activity

DIET

No research evidence supports the use of specific diets for mental retardation and/or Attention Deficit Hyperactivity Disorder (ADHD). Exception: Some metabolic and storage disorders, i.e., PKU.

PATIENT EDUCATION

Parental education and consultation as to the development of appropriate behavioral and educational expectations are strongly advised. Families should be referred to the local Association for Retarded Citizens.

FOLLOW UP

PREVENTION/AVOIDANCE

N/A

POSSIBLE COMPLICATIONS

Learning inappropriate behaviors

EXPECTED COURSE AND PROGNOSIS
  • Mild retardation: Social and communication skills appropriate for community functioning, basic job skills, and functional literacy
  • Moderate mental retardation: Speech deficits, social awareness, personal care skills, i.e., dressing, feeding, washing, sheltered employment, group home living
  • Severe mental retardation: Limited speech and language, poor motor development, in need of supervision
  • Profound mental retardation: Neurological defect, poor cognitive social ability, absent speech, possible self harm, extended care
  • Specific etiologies, i.e., Down syndrome and fragile X patients show a decline in cognitive and adaptive behavior over time

MISCELLANEOUS

ASSOCIATED CONDITIONS
  • Speech problems
  • Seizures
  • Maladaptive behaviors
  • Attention deficit hyperactivity disorder (ADHD):
    • Found with greater frequency among individuals with neuropsychological dysfunction
    • Treatment for ADHD among the mentally retarded is not unlike that for the "normal" population
    • Data indicates overuse of psychoactive substances to aid caretakers
AGE-RELATED FACTORS

Pediatric:N/A
Geriatric: N/A
Others: N/A

PREGNANCY

Parents and first degree relatives could benefit from consultation with a genetic associate or counselor

OTHER NOTES
  • Extensive family history to aid in diagnosis is mandatory
  • Genetic referral in cases without known etiology is appropriate
ABBREVIATIONS

MR = mental retardation

Clinical Investigations

ROLE OF HOMOEOPATHY

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