Structural chromosome aberrations cause swelling of the nucleus ...
Chromosome Aberrations in Humans
Transcript of Chromosome Aberrations in Humans
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ChromosomeAberrations In
Humans
-Archana Ramesh
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What are chromosomal aberrations?
A chromosome
anomaly, abnormality or aberration is a
missing, extra, or irregular portion
of chromosomal DNA.
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The various chromosomal aberrations
in humans
Chromosomal anomalies affect humans in the
form of a number of disorders.
Major disorders are:
1. Cri-du-chat Syndrome
2. Myelocytic Leukemia
3. Philadelphia Chromosome
4. Downs Syndrome
5. Chromosome 3 duplication-deletion syndrome
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Cri-du-Chat Syndrome
Also known as chromosome 5p deletionsyndrome, 5p minus syndrome orLejeunessyndrome.
Discovered by Jerome Lejeune and his colleagues.
Name of the syndrome came from a plaintive catlikemewing cry from small infants because of problems inthe larynx and nervous system.
Other characteristics include a small head, a saddlenose, broad face, widely shaped eyes with epicanthicfolds, unique facial features and mental retardation.
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IQs range from 20-40.
Chromosomal deficiency is in the short arm of
chromosome 5.
Patients suffering from this syndrome die early
and dont transmit, unless the deficiency gets
involved in reciprocal translocation.
5 translocates to 15, and carrier is a healthy
parent. If deficient member is carried, then
children exhibit it.
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Chronic Myelocytic Leukemia
Cancer of the blood producing cells of the bone marrowthat result in increasing wbcs.
Associated with the Philadelphia Chromosome, whichwas observed consistently in bone marrow preparations
of patients who had CML. A part of the long chromosome 22 translocated to
another chromosome, usually chromosome 9, leaving adeficiency behind.
Symptoms include enlarged spleen causing pain on theleft side, malaise, joint and/or hip pain, low-grade fever,increased susceptibility to infections, anemia,and thrombocytopenia with easy bruising
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CML is now largely treatedwith targeted drugscalled tyrosine kinase
inhibitors (TKIs), such asGleevec/Glivec (imatinib),Sprycel (dasatinib), Tasigna(nilotinib), Iclusig (ponatinib),or Bosulif (bosutinib) whichhave led to dramatically
improved long term survivalrates (95.2%) since theintroduction of Gleevec in2001. These drugs haverevolutionized treatment ofthis disease and allow most
patients to have a good qualityof life when compared to theformer chemotherapy drugs.
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Philadelphia chromosome
Philadelphia
chromosome or Philadelp
hia translocation is a
specific chromosomal abnormality that is associated
with chronic myelogenous
leukemia (CML). It is the
result of a
reciprocal translocation be
tween chromosome 9 and
22.
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Malignancy
Chromosomal abnormalities are increasing beingassociated with malignancies.
New staining methods are promoting more precisecomparisons of chromosomal arms and differentlystained sister chromatids.
Banded chromosome causes conditions like:
1. Burkitts Lymphoma
2. Tumor Retinoblastoma: Deletion of chromosome 13q.3. Wilms tumor
4. Bloom Syndrome
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Burkitts Lymphoma
Caused by translocation
of Chromosome 14.
Cancer of the Lymphatic
system.
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Wilms Tumor
Deletion in band 11p13.
Wilms
tumor or nephroblasto
ma is cancer ofthe kidneys that
typically occurs
in children, rarely
in adults.
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Bloom Syndrome
also known as BloomTorreMachacek
syndrome.
disorder characterizedby short stature andpredisposition to thedevelopment of cancer
Sister chromatidexchanges happenindicating instability.
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Downs Syndrome
Down syndrome disorders are based on having
too many copies of the genes located on
chromosome 21. In general, this leads to an over
expression of the genes. It is typically associated with physical
growth delays, a particular set of facial
characteristics and a severe degree of intellectualdisability. The average full-scale IQ of young
adults with Down syndrome is around 50.
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Downs Syndrome
The extra chromosome 21 material that causes Downsyndrome may be due to a Robertsonian translocation in thekaryotype of one of the parents. In this case, the long arm ofchromosome 21 is attached to another chromosome,often chromosome 14 .A person with such a translocation isphenotypically normal. During reproduction,normal disjunctions leading to gametes have a significantchance of creating a gamete with an extra chromosome 21,producing a child with Down syndrome. TranslocationDown syndrome is often referred to asfamilial Down
syndrome. It is the cause of 23% of observed cases ofDown syndrome.It does not show the maternal age effect,and is just as likely to have come from fathers as mothers.
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Chromosome 3 duplication-deletion
syndrome
This syndrome includes stillbirths, neonatal
deaths, and spontaneous abortions.
The children who survived this condition suffer
from facial malformation which includes:distorted head shape, thick, low eyebrows, low
hairline, long eyelashes, persistent lanugo,
distended veins on scalp, hypertelorism, a veryshort nose, protruding maxilla, etc.
Each infant has difficulty sucking and swallowing.
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Why translocation is not the bad guy?
It is not the translocation of the chromosome
that produces abnormalities, but rather the
imbalance of genetic material reflected in
chromosome deficiencies and duplicationsthat are produced by segregation of
translocation chromosome.
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BIBLIOGRAPHY
PRINCIPLES OF GENETICS
http://en.wikipedia.org/wik
http://www.ashg.org/
http://en.wikipedia.org/wikhttp://www.ashg.org/http://www.ashg.org/http://en.wikipedia.org/wik