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Genetic counseling: Mucopolysacharidosis (MPS)

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Mucopolysacharidosis (MPS)

ContractingEdit

  • Can you explain to me your main purpose in visiting genetics?
  • What are your main concerns about the diagnosis?
  • Outline session
  • First I will update the medical and family history
  • Doctor will then probably want to perform physical exam
  • Then we will address any concerns or questions

Medical historyEdit

  • Follow interim history form and focus on potential health problems/ symptoms described later in outline

Update PedigreeEdit

  • Any other brothers or sisters
  • Full biological?
  • Any other family members with:
  • Genetic conditions
  • Multiple miscarriages
  • Birth defects
  • Chronic illnesses
  • MR learning difficulties
  • Any chance that you and his father related by blood
  • Country where relatives are from originally

OverviewEdit

  • Group of inherited metabolic disorders
  • Caused by a deficiency of the specific lysosomal enzymes needed to break down mucopolysaccharides
  • Mucopolysaccharides are long chains of sugar molecules used to build connective tissues and organs in the body
  • When mutations occur in the genes for the enzymes that break down mucopolysaccharides, excess amounts of them are stored in the body
  • This causes progressive damage to organs and tissues
  • Eight clinical types and numerous subtypes have been identified
  • Although each type differs clinically, generally, people with mucopolysaccharidoses experience a period of normal development followed by a decline in physical and/or mental function
  • Some of the excess mucopolysaccharides are excreted through the urine and diagnosis often can be made through clinical examination and urine tests

IncidenceEdit

  • Estimated 1 in 25,000 births in U.S. have some form of MPS:

TreatmentEdit

  • No simple cure for the mucopolysaccharidoses
  • Treatment is symptomatic and supportive
  • In several individuals, bone marrow transplants have been attempted with varying degrees of success
  • Enzyme replacement trials (ERT) are under investigation for MPS I and MPS II
    • Kakkis et al. (2001) treated 10 patients with MPS I (aged 5 to 22 years) with recombinant human alpha-L-iduronidase at a dose of 125,000 U per kg of body weight given intravenously once weekly for 52 weeks.
    • Hepatosplenomegaly decreased significantly in all patients, and the size of the liver was normal for body weight and age in 8 patients by 26 weeks.
    • The rate of growth in height and weight increased by a mean of 85 and 131%, respectively, at 52 weeks in the 6 prepubertal patients.
    • The mean maximum range of motion of shoulder flexion and elbow extension increased significantly.
    • The number of episodes of apnea and hypopnea during sleep decreased by 61%.
    • New York Heart Association functional class improved by 1 or 2 classes in all patients.
    • Urinary glycosaminoglycan excretion decreased after 3 to 4 weeks of treatment; the mean reduction at 52 weeks was 63% of baseline values.
    • Five patients had transient urticaria during infusions. Serum antibodies to alpha-L-iduronidase were detected in 4 patients

ERTEdit

  • treatment consists of a modified form of the alpha-L-iduronidase enzyme given intravenously
  • takes approximately two hours for a person to receive the treatment, and the treatment is usually given every two weeks
  • Enzyme replacement therapy can stop and often reverse the symptoms of the disorder
  • Disadvantages of the enzyme replacement therapy are its high cost and the fact that it is a lifelong process
  • Potential adverse reactions including "allergic type reaction"
  • Initial evidence of potential treatment for Hurler syndrome (Keeling KM et al, 2001)
  • Gentamicin-mediated suppression of Hurler syndrome stop mutations restored a low level of alpha-L-iduronidase activity and reduced lysosomal glycosaminoglycan accumulation
  • results suggest that the suppression of premature stop mutations may provide an effective treatment for Hurler syndrome patients with premature stop mutations in the IDUA gene

Types of MPSEdit

  • MPS type I
    • Hurler, Scheie, and Hurler/Sheie syndromes also known respectively as MPS-IH, MPS-IS, and MPS-IH/S
    • Hurler syndrome takes its name from Gertrud Hurler, the doctor who described a boy and girl with the condition in 1919
    • In 1962, Dr. Scheie, a consultant ophthalmologist, wrote about some of his patients who were more mildly affected
    • Patients who seem not to fit clearly in either the severe or the mild end of the disorder are said to have *Hurler/Scheie syndrome
    • All are caused by missing enzyme - alpha-L-iduronidase
    • Alpha-L-iduronidase breaks down (mucopolysaccharides) heparan sulfate and dermatan
    • Found at locus 4p16.3
    • No reliable way of telling from biochemical tests how severe the disorder will be
    • residual alpha-L-iduronidase activity in Hurler fibroblasts is heat-stable whereas that in Scheie fibroblasts is heat-labile
    • Progression and severity of disease are highly variable within the spectrum of MPS)

General symptomsEdit

  • multiple organ and tissue involvement
  • Joint stiffness
  • Skeletal deformities
  • Enlarged liver
  • Obstructive airway disease; respiratory infection and cardiac complications are the most common direct causes of death
  • Ophthalmologic manifestations and hearing disorders

Three subgroups of MPSI according to severityEdit

  • Sheie syndrome
  • corneal opacities
  • aortic valve disease
  • normal stature
  • mild or absent intellectual impairment
  • nearly normal life span
  • seldom recognized during infancy or early childhood
  • No neurologic involvement
  • Joint stiffness, carpet tunnel syndrome
  • Mild hepatosplenomegaly
  • Hurler/Sheie
    • Onset of symptoms between 3 and 8 years of age
    • death in 2nd or 3rd decade normal or near normal intelligence
    • more severe physical symptoms than those with Scheie syndrome
    • short stature
    • dysostosis multiplex
    • hepatosplenomegaly
    • corneal clouding
    • umbilical or inguinal hernia
    • psychotic symptoms may appear later in life
  • Hurler syndrome
    • Most severe form
    • Occurs in infancy
    • Macrocephaly (*may appear early in infancy while complete clinical picture develops during second year of life)
    • Respiratory infections*
    • Limited hip abduction*
    • Apnea or difficulty breathing
    • Coarse (gargyloid) facies
    • accelerated growth from infancy followed by progressive decline in the rate of development
    • progressive physical disability
    • progressive mental retardation
    • dysostosis multiplex
    • corneal clouding
    • death usually before the age of 10 years usually result of pneumonia and heart failure

Inheritance and risksEdit

  • AR inheritance, panethnic
  • Parents of affected child have ¼ chance of each pregnancy being affected
  • Unaffected sibs of patient have 2/3 chance of being carrier
  • Combined frequency: approximately 1 in 50,000
    • Hurler: 1 in 100,000
    • Hurler-Scheie: 1 in 115,000
    • Scheie: 1 in 500,000

DiagnosisEdit

  • can be diagnosed with a blood looking at levels of alpha-L-iduronidase
  • low level of this enzyme in a person's white blood cells is characteristic of the disease
  • confirmed by this absence of alpha-L-iduronidase in the white blood cells, the excretion of dermatan sulfate and heparan sulfate in the urine, and by physical appearance
  • Molecular (DNA) analysis can also be used to verify the diagnosis

Genetic TestingEdit

  • Prenatal diagnosis
  • possible once a diagnosis has been made in the family and a genetic alteration identified (CVS and
  • amount of alpha-L-iduronidase can be measured in the amniotic cells or chorionic villi Molecular (DNA) analysis can be used to verify the diagnosis prenatally, by looking for the same genetic alteration that is present in the family member
  • Carrier testing
  • Enzyme analysis using white blood cells is not effective or reliable in identifying carriers of these disorders
  • However, a study in 2002 (Mandelli J et al) showed that leukocyte IDUA from MPS I heterozygotes differed from the normal enzyme in terms of optimum pH, Km, and Vmax of the reaction and thermostability at 50 degrees C. They claimed these parameters provide a simple and reliable tool for the detection of carriers for MPS I.
  • molecular (DNA) analysis is used to identify carriers
  • first test someone in the family who has already been diagnosed with the disorder, so that the laboratory can identify the genetic alteration present in that individual and look for that same alteration in at-risk family members

MPS II (Hunter syndrome -differential diagnosis)Edit

OverviewEdit

  • named after Charles Hunter, the professor of medicine in Manitoba, Canada, who first described two brothers with the disorder in 1917
  • Hunter syndrome is less common than MPS I and has no corneal clouding and pursues a slower course than MPS I
  • Some think there are two distinct types of the condition, the mild and the severe
  • Others believe there is just one disorder with a wide range in the severity of the problems it causes

Risks and inheritanceEdit

  • X-linked recessive
  • Rarely girls have been diagnosed
  • Mother of affected boy is carrier
  • 50% risk to future boys
  • maternal aunts and sisters at risk of being carrier
  • carrier testing available

Description of symptomsEdit

  • Severe form:
    • Joint stiffness
    • Mental deterioration
    • Dwarfing
    • Progressive deafness
    • Death by age 15
  • Mild form:
    • Short stature
    • Limitation of motion
    • Enlarged forehead, tongue and lips
    • Life span may be normal

Other DifferentialsEdit

  • MPS III,or Sanfilippo syndrome
    • experience progressive dementia and mental deterioration in childhood
    • Death usually occurs in the late teens
  • MPS IV,or Morquio syndrome
    • Symptoms usually appear in infancy and may include severe dwarfing and corneal clouding
    • Intelligence is normal
    • Cardiac or respiratory disease may cause death in the third or fourth decade of life
  • MPS VI,or Maroteauz-Lamy syndrome
    • resembles Hurler syndrome
    • Onset is in infancy
    • intelligence is normal
    • Individuals may live into the second or third decade
  • MPS VII, Sly disease
    • experience corneal clouding, skeletal irregularities, and enlargement of the liver and spleen
    • Intellectual impairments vary for this type of MPS

Drug-induced lysosomal storage diseaseEdit

  • example of phenocopy
  • thought that drugs of widely differing pharmacologic activity can interact with polar lipids within the lysosomes to yield lipid-drug complexes resistant to enzymatic digestion

Psychosocial considerationsEdit

  • Assess how this disease is viewed by patient and family members
  • Probably difficult to watch progression of disease may feel helpless
  • May seek out every possible therapy (including alternative med. tx)
  • Difficulty accepting that life-span may be shortened
  • May have been overprotected by parents
  • May struggle with feelings of dependence on others
  • Discuss support group

Support and Information OrganizationsEdit

  • National MPS Society, Inc.
102 Aspen Drive
Downingtown, PA 19335
info@mpssociety.org
http://www.mpssociety.org
Tel: 610-942-0100
Fax: 610-942-7188
  • National Organization for Rare Disorders (NORD)
P.O. Box 1968
(55 Kenosia Avenue)
Danbury, CT 06813-1968
orphan@rarediseases.org
http://www.rarediseases.org
Tel: 203-744-0100 Voice Mail 800-999-NORD (6673)
Fax: 203-798-2291
  • National Tay-Sachs and Allied Diseases Association
2001 Beacon Street
Suite 204
Boston, MA 02135
NTSAD-boston@worldnet.att.net
http://www.ntsad.org
Tel: 617-277-4463 800-90-NTSAD (906-8723)
Fax: 617-277-0134
http://www.ninds.nih.gov/health_and_medical/disorders/mucopolysaccharidoses.htm --National Institute of Neurological :Disorders and Stroke

ReferencesEdit

NotesEdit

The information in this outline was last updated in 2002.


This material has been imported fom the wikibook "Genetic counseling"[ http://en.wikibooks.org/wiki/Genetic_counseling] under the GNU Free Documentation License.

Heckert GNU white Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled "GNU Free Documentation License."

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