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Genetic counseling: Balanced Translocation

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Balanced Translocation

Introduction and ContractingEdit

  • Can you explain in your own words what you understand about why you were referred to genetics?
  • What are your main concerns for ______ at this time?
  • Do you have any specific questions you would like us to make sure we try to answer?

Outline sessionEdit

  • Take medical and family history
  • Review the chromosome results with you
  • Explain more about why we want to do chromosome testing on you (parents)
  • Dr Viskochil will examine him
  • We will then make sure to discuss any further questions or concerns

Medical/Developmental HistoryEdit

  • follow form that I started filling out and confirm info

Family HistoryEdit

  • 3 generation pedigree
  • include standard questions don't forget miscarriages as they occur more frequently in people with balanced translocation

Explain Chromosomes and Genes (using sample karyotype)Edit

  • When the lab looked at _____ 's cells under a microscope they found a change in the chromosomes
  • The change they found was called a translocation

What is a translocation?Edit

  • Transfer of chromosomal material between chromosomes

Why do translocations happen?Edit

  • We do not really know why
  • Estimated that about 1 person in 500 has a chromosome translocation
  • We know that our chromosomes seem to break and rejoin quite often, and it is only sometimes that it leads to problems
  • These changes are out of our control, and nearly always translocations happen in either the egg or sperm cell before they join together
  • Therefore they are not likely to be caused by anything during the pregnancy

How Translactions OccurEdit

  • Sometimes the chromosomes break during cell division and are usually repaired
  • Sometimes two fragments may break off from two different chromosomes, and "swap" places
  • This is called a reciprocal translocation (this is the type of translocation he has)

Show Karyotype and Explain Specific Break PointsEdit

  • Sometimes helps to see the actual karyotype
  • 46 means that the usual number of chromosomes is present
  • Y chromosome is what makes him male
  • T stands for translocation, where a piece of chromosome 2 and 21 exchanged places
  • The rest just tells us more exactly where the chromosomes broke
  • So arrows are pointing to where the chromosomal material exchanged places

Balanced TranslocationsEdit

  • In most cases, there is no loss or gain of chromosomal material during the exchange process
  • When the lab looked they didn't see any missing or extra pieces of chromosomes and they therefore think that this might be a balanced translocation

What Are the EffectsEdit

  • Often people will have a balanced translocation and not even know because they don't experience any problems (this occurs in majority of cases of new balanced rearrangements Warburton 1991)
  • Sometimes, apparently balanced translocation carriers show some characteristics or symptoms (Warburton showed that frequency of abnormality was 6.1% but confidence interval includes 3% in apparently balanced translocations)
  • One explanation for this finding is that the break may have occurred in the middle of a gene that is important in growth or development and the gene no longer provides correct instructions because it is disrupted
  • We do not know if this translocation is the explanation for the characteristics and health problems in ______

What will results from parental chromosomes tell usEdit

  • In order to determine what the translocation might mean it is important to do chromosomes on all parents of children with a translocation
  • If a parent has the same translocation and they do not have any of the same symptoms or characteristics as the child than we cannot conclude that the translocation is the cause
  • If neither parent has the translocation than it may explain some or all of the characteristics and health problems in ______, but would be difficult to know for certain
  • Parental chromosomes will also be important because it will help us determine what risks might be to future offspring

What can happen in offspring of people with balanced translocationEdit

  • If one of the parents carries a balanced translocation, it is possible for a child of theirs to acquire a bit of extra chromosome material or a bit missing
  • Either of these would be known as an UNBALANCED translocation
  • This extra and or missing pieces of chromosome can unfortunately cause serious mental, physical and medical challenges in the child who inherits them
  • Sometimes they cause a miscarriage, but not always
  • However, it is also possible for these same parents to have a child with normal chromosomes, or a child with the same balanced rearrangement of their chromosomes as the parent
  • Having a balanced translocation of your chromosomes does not mean you cannot have normal healthy children
  • Factors that influence risks (not applicable in this case)
  • Ascertainment - A family ascertained as a result of a previously affected child is seen to be at increased risk of recurrence since the inbalance has been proved viable.
  • Risk of having an affected child is lower when a family is ascertained following for example repeated spontaneous miscarriage since in these cases the imbalance is more likely to be inviable
  • Each time they have a child, there are several possibilities.
    • they may have a child with normal chromosomes
    • they may have a child with the same balanced rearrangement of the chromosomes as the parent
    • they may have a child with an unbalanced rearrangement of the chromosomes which may cause mental and physical challenges
    • the pregnancy may end in a miscarriage

What sort of problems do unbalanced translocations cause?Edit

  • Can be difficult to predict because it depends on:
  • Which parts of chromosomes are missing or duplicated (aneuploidy for 4p, distal 4q and 9p for example all have a high degree of viability therefore relatively high risk)
  • how large of pieces they are (if large less likely to be viable due to more extra or missing information)
  • There are not usually the same breaking points for each translocation because it is random so we don't have any other children to compare this exact translocation to
  • Nearly always have learning problems though if translocation is unbalanced

Tests in Pregnancy for Translocation CarriersEdit

  • amniocentesis This is usually done from 14 weeks in the pregnancy and the result normally takes about 2 weeks.
  • Chorionic villus sampling (CVS) usually done between 10-12 weeks in the pregnancy, and the results take about 2 weeks.

Psychosocial ConsiderationsEdit

  • Information can be difficult to understand because translocations are not an easy concept
  • Don't expect them to remember everything, we will provide a summary in a letter we will write
  • People who have a balanced translocation of their chromosomes do not have a disease that can be "caught" by other people
  • Guilt about possibly passing this on (not under our control can't cause or prevent)
  • What do other family members know and do you plan on telling them
  • Either parent considering having more children because this may alter their plans or could be upsetting to think they may have a recurrence risk if they didn't think so before

References and Patient ResourcesEdit

NotesEdit

The information in this outline was last updated in 2002.



Material obtained under GFDL Licence from http://en.wikibooks.org/wiki/Handbook_of_Genetic_Counseling

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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