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Neurological Bases of Behavior (PSY610) 
Assignment No. 01 
Due Date: 23.05. 2014 Marks: 20 

Assignment Objective 

Upon completion of this assignment, students will be able to understand the physical and behavioral 
characteristics of people having chromosomal abnormalities. 

Dear Students, 

Given below are five case scenarios. In each scenario there is description of one type of chromosomal 
abnormality. You are required to read the following cases carefully and specify the chromosomal 
abnormality portrayed in each case along with the justification of your answer. 

1. Ali had a small flat nose, larger tongue, upturned eyes and small ears at the time of birth. His 
face was almost rounded in shape. At the age of 3 months, he was not able to follow the objects 
with his eyes. His parents know this fact that such type of activity can easily be performed by 
the child of 3-months. Moreover, when he reached at the age of 6 months, he was not able to 
grasp the toys. 
2. Amjad at the age of 6 years was physically different as compared to the other boys of his age. 
He had slightly weaker muscles and had slower motor coordination. When he reached at his 
puberty age, his breasts started to grow. He had very sparse body hair and usually he used to 
keep quiet in social gatherings. When he got married, his doctors told that he can never become 
a father due to the inability to make sperms. 
3. Afifa, 25 years old woman is having a short stature, webbed neck and kidney problems. After 
getting married, she was unable to conceive a baby because her ovaries were not developed 
properly. Additionally, she faced some problems regarding right-left directional discrimination 
and experiences difficulty in copying figures. 
4. Aslam, a 20 years old young man had a strong muscular tone. He had some temperamental 
problems and usually became aggressive on small things. He did not comply with the social 
norms and became rude and violent in his actions. He has been sentenced in jail for two years 
because he has murdered his class fellow on a very trivial matter. After killing him he sliced 
the dead body into many pieces. His parents were extremely worried due to his behavior. They 
visited a doctor and tend to probe the reason of such behavior. His doctor told that; he suffered 
from chromosomal abnormality. 
5. Atif, an infant of 2-years old has low muscle coordination. He is unable to sit properly. 
Sometimes, he shows involuntary movements of his body. He is habitual of chewing his lips 
and his mouth. His parents are too much worried about his delayed and inappropriate developmental milestones and consult a doctor. His doctor suspects about the abnormality in 
• Do not include unnecessary details in justification. Keep your answer to the point. 
• Only use the table given below for attempting this assignment. 

Marking Scheme: 1 mark for the identification of each chromosomal abnormality and 3 marks for 
the justification of that selection. 

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chromosome anomalyabnormalityaberration, or mutation is a missing, extra, or irregular portion of chromosomal DNA.[1] It can be from an atypical number of chromosomes or a structural abnormality in one or more chromosomes. Akaryotype refers to a full set of chromosomes from an individual that can be compared to a "normal" karyotype for the species via genetic testing. A chromosome anomaly may be detected or confirmed in this manner. Chromosome anomalies usually occur when there is an error in cell division following meiosis ormitosis. There are many types of chromosome anomalies. They can be organized into two basic groups, numerical and structural anomalies.

The majority of known types of chromosomal abnormalities involve sex chromosomes.  In frequency of occurrence, they are only slightly less common than autosomal abnormalities.  However, they are usually much less severe in their effects.  The high frequency of people with sex chromosome aberrations is partly due to the fact that they are rarely lethal conditions.  Like Down syndrome and other autosomal problems, sex chromosome gross abnormalities can be diagnosed before birth by amniocentesis and chorionic villi sampling.

Sex chromosome abnormalities are gender specific.  Normal males inherit an X and a Y chromosome while females have two X's.  A single Y chromosome is sufficient to produce maleness while its absence is necessary for femaleness.  Female abnormalities are due to variations in the number of X chromosomes.  Male abnormalities are the result of irregular numbers of either the X or the Y chromosome or both.  

Turner syndrome click this icon to hear the preceding term pronounced occurs when females inherit only one X chromosome--their genotype is X0 (i.e., monosomy X).  If they survive to birth, these girls have abnormal growth patterns.  They are short in stature, averaging 4 foot 7 inches as adults, and often have distinctive webbed necks (i.e., extra folds of skin), small jaws, and high arched palates.  They generally lack prominent female secondary sexual characteristics.  They have exceptionally small, widely spaced breasts, broad shield-shaped chests, and turned-out elbows.  Their ovaries do not develop normally and they do not ovulate.  The few oöcytes that they produce are destroyed by the time they are two.  They are in a sense postmenopausal click this icon to hear the preceding term pronounced from early childhood and are sterile.  However, they can become pregnant and give birth if fertilized eggs from a donor are implanted.  Women with Turner syndrome have a higher than average incidence of thyroid disease, vision and hearing problems, heart defects, diabetes, and other autoimmune disorders.  In a fewindividuals, there is slight mental retardation.  Turner syndrome is rare.  Current estimates of its frequency range from 1 in 2,000 to 1 in 5,000 female infants.  If diagnosed in early childhood, regular injections of human growth hormones can increase their stature by a few inches.  Beginning around the normal age of puberty, estrogen replacement therapy can result in some breast development and menstruation.  These treatments allow Turner syndrome women to appear relatively normal.

Triple-X syndrome occurs in women who inherit three X chromosomes--their genotype is XXX or more rarely XXXX or XXXXX. As adults, these "super-females" or "metafemales" click this icon to hear the preceding term pronounced, as they are sometimes known, generally are an inch or so taller than average with unusually long legs and slender torsos but otherwise appear normal.  They usually have normal development of sexual characteristics and are fertile but tend to have some ovary abnormalities that can lead to premature ovarian failure.  They may have slight learning difficulties, especially in speech and language skills, and are usually in the low range of normal intelligence (especially the XXXX and XXXXX individuals).  They frequently are very tall in childhood and tend to be emotionally immature for their size.  This sometimes results in teachers and other adults labeling them as troublemakers because they expect more maturity from bigger girls.  However, they are usually as emotionally mature as other girls of their age.  None of these traits prevent them from being socially accepted as ordinary adult women.  Individuals who are genetic mosaics (XX/XXX) have less noticeable symptoms.  Triple-X syndrome is less rare than Turner syndrome, but little is known about it.  The frequency is approximately 1 in 1,000 female infants and it occurs more commonly when the mother is older. 

Klinefelter syndrome click this icon to hear the preceding term pronounced males inherit one or more extra X chromosomes--their genotype is XXY or more rarely XXXY or XY/XXY mosaic.  In severe cases, they have relatively high-pitched voices, asexual to feminine body contours as well as breast enlargement, and comparatively little facial and body hair.  They are sterile or nearly so, and their testes and prostate gland are small.  As a result, they produce relatively small amounts of testosterone.  The feminizing effects of this hormonal imbalance can be significantly diminished if Klinefelter syndrome boys are regularly given testosterone from the age of puberty on.  Like triple-X females(described above), many Klinefelter syndrome men are an inch or so above average height.  They also are likely to be overweight.  They usually have learning difficulties as children, especially with language and short-term memory.  If not given extra help in early childhood, this often leads to poor school grades and a subsequent low self esteem.  However, most men who have Klinefelter syndrome are sufficiently ordinary in appearance and mental ability to live in society without notice.  It is not unusual for Klinefelter syndrome adults with slight symptoms to be unaware that they have it until they are tested for infertility.  They are usually capable of normal sexual function, including erection and ejaculation, but many, if not most, are unable to produce sufficient amounts of sperm for conception.  Klinefelter syndrome males with more than two X chromosomes usually have extreme symptoms and are oftenslightly retarded mentally.  Men who are mosaic (XY/XXY) generally have the least problems.  There is no evidence that Klinefelter syndrome boys and men are more inclined to be homosexual, but they are more likely to be less interested in sex.  They have a higher than average risk of developing osteoporosis, diabetes, and other autoimmune disorders that are more common in women.  This may be connected to low testosterone production.  Subsequently, regular testosterone therapy is often prescribed.  The frequency of Klinefelter syndrome has been reported to be between 1 in 500 and 1 in 1000 male births.  This makes it one of the most common chromosomal abnormalities.   Males with Down syndrome sometimes also have Klinefelter syndrome.  Both syndromes are more likely to occur in babies of older mothers.

XYY syndrome click this icon to hear the preceding term pronounced males inherit an extra Y chromosome--their genotype is XYY.  As adults, these "super-males" are usually tall (above 6 feet) and generally appear and act normal.  However, they produce high levels of testosterone.  During adolescence, they often are slender, have severe facial acne, and are poorly coordinated.  They are usually fertile and lead ordinary lives as adults.  Many, if not most, are unaware that they have a chromosomal abnormality.  The frequency of XYY syndrome is not certain due to statistical differences between different studies.  It may be as common as 1 in 900 male births to as rare as 1 in 1500 or even 1 in 2,000.  XYY syndrome is also referred to as Jacobs syndrome. 

Early studies of XYY syndrome done in European prisons initially led to the erroneous conclusion that these men were genetically predisposed to antisocial, aggressive behavior, below average intelligence, and homosexuality.  Contributing to the early view that XYY syndrome men have serious personality disorders was the case of Richard Speck.  In 1966, he coldly murdered 8 nurses in a Chicago dormitory.  At his trial, his lawyer claimed that he was innocent due to uncontrollable urges caused by his XYY genotype.  This novel appeal was akin to claiming insanity or severely diminished mental competence.  The jury was not convinced and found him guilty of murder.  He was sentenced to life in prison where he eventually died.  In fact, Richard Speck did not have an XYY genotype.  However, some researchers suggest that the high testosterone levels of XYY men can make them somewhat more prone to violence and that this may cause higher rates of wife beating.


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