Term
Chromosome abnormalities are present in about 1/____ live births. |
|
Definition
|
|
Term
Chromosome abnormalities are the leading cause of both ______________ and ____________. |
|
Definition
Mental retardation and pregnancy loss. |
|
|
Term
Chromosome abnormalities are seen in what percentage of first and second trimester spontaneous abortions? |
|
Definition
|
|
Term
What 3 main techniques has improved the visualizations of chromosomes (starting in the 1950s)? |
|
Definition
spindle poisons to arrest cells in metaphase, hypotonic solutions to swell nuclei, and staining techniques to bring out the chromosome banding patterns |
|
|
Term
What special features are seen on the short arms of acrocentric chromosomes? |
|
Definition
|
|
Term
What does 14q32.3 refer to? |
|
Definition
The 3rd sub-band, of band 2, of the third region of the long arm of chromosome 14. |
|
|
Term
What was the first banding stain? |
|
Definition
|
|
Term
What is the most popular banding stain, and what must be done before its application? |
|
Definition
Giemsa staining (G-banding), applied after chromosomes are partially digested by trypsin |
|
|
Term
What is reverse banding and what is it good for? |
|
Definition
It requires heat treatment and reverses the typical black and white banding patterns, helpful for the distal ends of chromosomes. |
|
|
Term
What stains the constitutive heterochromatin which usually lies near centromeres? |
|
Definition
|
|
Term
What does NOR staining do? |
|
Definition
highlights the stalks and satellites of acrocentric chromosomes |
|
|
Term
What type of banding is used to look for a specific, subtle chromosomal abnormality? |
|
Definition
High-resolution banding, done during prophase or early metaphase, increases observable bands to as many as 800. |
|
|
Term
|
Definition
Fluorescent in-situ hybridization, labeled probe is hybridized with chromosomes and observed under fluorescence microscope for added, deleted or rearranged material |
|
|
Term
What is spectral karyotyping? |
|
Definition
Different fluorescent probes are used to paint chromosomes, very helpful for rearrangements. |
|
|
Term
What is comparative genomic hybridization, CGH? |
|
Definition
A test source of DNA is labeled one color, a normal control DNA source is labeled another, they are hybridized to normal metaphase chromosomes. Especially helpful in scanning for deletions or duplications in cancer cells. |
|
|
Term
A cell with a number of chromosomes that is a multiple of 23 is said to be... |
|
Definition
|
|
Term
_______ is the presence of a complete set of extra chromosomes in a cell. |
|
Definition
|
|
Term
Triploidy is seen in 1/_____ live births, and accounts for ___% of chromosomal abnormalities occurring at conception. |
|
Definition
|
|
Term
What is the most common cause of triploidy? |
|
Definition
Fertilization by two sperm, dispermy |
|
|
Term
The fusion of an ovum and polar body and subsequent fertilization by a sperm would cause... |
|
Definition
|
|
Term
Meiotic failure, in which a diploid sperm or egg is produced, could produce which zygotic condition? |
|
Definition
|
|
Term
A mitotic failure in the early embryo, in which all the duplicated chromosomes go to one daughter cell, could cause what condition in the zygote? |
|
Definition
|
|
Term
The fusion of two diploid zygotes could cause... |
|
Definition
|
|
Term
What does aneuploid refer to? |
|
Definition
A cell that does not contain a multiple of 23 chromosomes. |
|
|
Term
In terms of live births, compare autosomal monosomies to trisomies? |
|
Definition
Only a few monosomies have been observed among live births, trisomies are more common |
|
|
Term
What is the most common cause of aneuploidy? |
|
Definition
|
|
Term
Nondisjunction can cause offspring to have what condition(s)? |
|
Definition
|
|
Term
What is the most common aneuploid condition compatible with survival? |
|
Definition
Down syndrome, trisomy 21 |
|
|
Term
Trisomy 21 is seen in 1/____ live births. |
|
Definition
|
|
Term
Who originally described Down syndrome, and when? |
|
Definition
|
|
Term
Describe the typical features of Down syndrome. |
|
Definition
Low nasal bridge, upslanting palpebral fissures, epicanthic fold, small and sometimes overfolded ears, flattened maxillary and malar region, round cheeks, corners of the mouth are sometimes downturned, short neck, redundant nuchal fold, flat occiput, broad and short hands and feet, simian crease in 50%, hypotonia (highly consistent) |
|
|
Term
Which types of GI issues will develop in 3% of infants with trisomy 21? |
|
Definition
Duodenal obstruction, atresia of esophagus, duodenum or anus. |
|
|
Term
Common respiratory infections and an increased risk of leukemia (15-20x) are seen in children with which condition? |
|
Definition
|
|
Term
What proportion of children with Down syndrome are born with structural heart defects? |
|
Definition
|
|
Term
What is the most common heart defect in children with Down syndrome, and what does it cause? |
|
Definition
AV canal, the septa failed to fuse so blood flows from left to right side of the heart, then to pulmonary vasculature, producing pulmonary hypertension |
|
|
Term
Ventricular septal defects are common among babies with... |
|
Definition
|
|
Term
Which condition accounts for 10% of all cases of mental retardation in the US? |
|
Definition
Down syndrome, moderate to severe retardation is seen in most individuals (IQ of 25-60) |
|
|
Term
In young children with Down syndrome, what are some of the most important health issues to watch for? |
|
Definition
Conductive and sometimes neural hearing loss, hypothyroidism, various eye abnormalities |
|
|
Term
It is estimated that __% of children with Down syndrome will survive to age 10. |
|
Definition
|
|
Term
Males with Down syndrome are nearly always... |
|
Definition
|
|
Term
Some females with Down syndrome can reproduce, although approx. __% fail to ovulate. |
|
Definition
|
|
Term
Approx. __% of trisomy 21 conceptions are spontaneously aborted. |
|
Definition
|
|
Term
Approx 95% of Down syndrome cases are caused by ______. About 75% of the time, this occurs during _______. |
|
Definition
nondisjunction, meiosis 1. |
|
|
Term
Mosaicism is seen in approx. __ - ___% of trisomy 21 live births. |
|
Definition
|
|
Term
What would the notation look like for a male with trisomy 21 mosaicism? |
|
Definition
|
|
Term
What is the most common cause for mosaicism of a trisomy? |
|
Definition
trisomic conception followed by loss of the extra chromosome during early mitosis of the embryo |
|
|
Term
The occurrence of germ-line mosaicism trisomy 21 helps account for the recurrence risk for Down syndrome among mothers under 30 yrs old, which is __%. |
|
Definition
|
|
Term
What is the critical portion of chromosome 21 responsible for Down syndrome? |
|
Definition
|
|
Term
Which hormone(s) should be measured annually in kids with Down syndrome? |
|
Definition
|
|
Term
Why should imaging studies be done in older kids with Down syndrome who want to participate in athletic activities? |
|
Definition
Instability of the first and second vertebrae has led to spinal cord injuries in some |
|
|
Term
The cause of mental retardation in Down syndrome has been localized to which gene in the critical region? |
|
Definition
|
|
Term
APP encodes which protein? What does it cause? |
|
Definition
amyloid beta precursor protein, triple copy is likely to account for Alzheimer-like dementia in nearly all Down syndrome pts by age 35-40. (mutations in this gene also cause a small number of Alzheimer disease cases) |
|
|
Term
Which trisomy is also known as Edwards syndrome? Of autosomal trisomies, how common is it? What is the incidence among live births? |
|
Definition
Trisomy 18, second most common, 1/6000 |
|
|
Term
Describe the incidence of Edwards syndrome among stillbirths with congenital malformations. |
|
Definition
It is the most common chromosome abnormality among stillborns with congenital malformations, therefore it is much more common at conception than among live births |
|
|
Term
Which chromosomal abnormality causes prenatal growth deficiency, characteristic facial features, distinctive hand abnormality, small ears with unraveled helices, small mouth that can be hard to open, short sternum, short big toes, heart defects, omphalocele, diaphragmatic hernia and occasionally spina bifida? |
|
Definition
|
|
Term
Those with __________ who survived infancy have marked developmental infancy and most are not able to walk. |
|
Definition
|
|
Term
More than 95% of those with Edwards syndome have a complete _________. Small percentage have _______. |
|
Definition
|
|
Term
As in trisomy 21, there is a significant maternal age effect with ________, and approx 90% of these cases are the result of an extra chromosome contributed from the _________. |
|
Definition
|
|
Term
This condition, also called Patau syndrome, is seen in about 1/______ births. |
|
Definition
|
|
Term
The malformation pattern in this condition is distinctive for oral-facial clefts, micropthalmia, postaxial polydactyly, malformations of the CNS and cutis aplasia. |
|
Definition
|
|
Term
The survival rate for _________ is similar to that for Trisomy 18, with ____% of pts dying within the first year of life. |
|
Definition
|
|
Term
As in trisomy 18, those with trisomy 13 who survive infancy have significant... |
|
Definition
developmental retardation |
|
|
Term
About __% of causes of Patau syndrome have a full ______. Most of the remaining cases have ______ of the ____ arm of chromosome ___ due to a translocation. |
|
Definition
80, trisomy 13, trisomy, long, 13 |
|
|
Term
The risk of bearing a child with trisomy 13 increases with... |
|
Definition
|
|
Term
Is it estimated that ___% or more of trisomy 13 and 18 conceptions are spontaneously lost during pregnancy. |
|
Definition
|
|
Term
Among mothers under the age of 30, the risk of Down syndrome is less than 1/_____. At age 35, it is 1/____. At age 40, 1/____. After age 45, 1/____. |
|
Definition
|
|
Term
Approximately ___% of children with Down syndrome are born to mothers under the age of 35. |
|
Definition
|
|
Term
Describe the paternal age affect for trisomies. |
|
Definition
If it exists at all, it is minor. |
|
|
Term
Among live births, about 1/___ males and 1/___ females have some form of sex chromosome aneuploidy. |
|
Definition
|
|
Term
What is Turner syndrome? What are the major findings? |
|
Definition
45,X. 1) proportionate short stature, 2) sexual infantilism and ovarian dysgenesis, 3) pattern of major and minor malformations |
|
|
Term
What syndrome causes a triangle-shaped face, posteriorly rotated external ears and a broad webbed neck? |
|
Definition
|
|
Term
What do infants with Turner syndrome sometimes display on the hands and feet? |
|
Definition
|
|
Term
What defects of vital organs are seen in Turner syndrome? |
|
Definition
Congenital heart defects, structural kidney defects |
|
|
Term
Describe the mental retardation of Turner syndrome. |
|
Definition
Pts are not mentally retarded. |
|
|
Term
Girls with Turner syndrome do not undergo an adolescent ______________. Instead of ovaries, they usually have ________. They usually do not develop _____________, but can be treated with _________ for this. |
|
Definition
growth spurt, connective tissue streaks, secondary sexual characteristics, estrogen |
|
|
Term
Chromosomal abnormalities of Turner syndrome are quite variable, ___% to ___% are mosaics, most commonly ________ and less commonly _______. |
|
Definition
30-40%, 45,X/46,XX, 45,X/46,XY |
|
|
Term
Turner syndrome mosaics who have ___ chromosomes in some cells are predisposed to developing _____________. |
|
Definition
Y, malignancies of gonadal streaks |
|
|
Term
About 10-20% of pts of Turner syndrome have structural abnormalities of the X chromosome involving a... |
|
Definition
deletion of some or all of the short arm. |
|
|
Term
Approx 80% of monosomy X cases are caused by meiotic error in the... |
|
Definition
|
|
Term
Only about 1/2500 to 1/5000 live born females have this disorder. |
|
Definition
|
|
Term
The 45,X karyotype accounts for ___% to ___% of the chromosome abnormalities seen among spontaneous abortions. |
|
Definition
|
|
Term
What percentage of 45,X conceptions are lost prenatally? |
|
Definition
|
|
Term
What type of mosaicism is especially common among 45,X pts who survived to term? |
|
Definition
confined placental mosaicism |
|
|
Term
In Turner syndrome, mutations in the ______ gene produce short stature. It's located at the distal tips of the __ and __ short arms (the _________ region). |
|
Definition
SHOX, X and Y, pseudoautosomal |
|
|
Term
How do females with Turner syndrome who received the X chromosome from their father differ from those who got it from mom? |
|
Definition
Higher verbal IQ scores and better social cognition |
|
|
Term
The imprinted region of the X chromosome escapes... |
|
Definition
|
|
Term
What is the karyotype of Klinefelter syndrome? What is the incidence among births of the correct gender? |
|
Definition
47,XXY, 1/1000 male births |
|
|
Term
Klinefelter syndrome is a primary cause of _________________ in this gender. |
|
Definition
|
|
Term
Males with this syndrome tend to be taller than average, have disproportionately long arms and legs, small testes, sterility from atrophy of seminiferous tubules and gynecomastia. |
|
Definition
|
|
Term
Describe the intellect of those with 47,XXY. |
|
Definition
Predisposition or learning disabilities and sub-average intelligence, but pts are not usually mentally retarded |
|
|
Term
The extra X chromosome in 47,XXY comes from the mom in ___% of cases, and the condition increases with increased maternal age. |
|
Definition
|
|
Term
Mosaicism is seen in about __% of pts with Klinefelter syndrome. |
|
Definition
|
|
Term
At least __% of conceptions with 47,XXY are spontaneously aborted. |
|
Definition
|
|
Term
With each extra X chromosome, what increases? |
|
Definition
degree of mental deficiency and physical abnormality |
|
|
Term
What kind of therapy can enhance secondary sex characteristics in males with ______ syndrome? |
|
Definition
testosterone, Klinefelter |
|
|
Term
The ________ karyotype occurs in approx 1/1000 females and usually has a benign phenotype. |
|
Definition
|
|
Term
Trisomy X females sometimes suffer from... |
|
Definition
sterility, menstrual irregularity, mild mental retardation |
|
|
Term
The great majority of cases of trisomy X are the result of _________ in the ________. |
|
Definition
|
|
Term
Males with this karyotype tend to be taller than average and have subaverage intelligence. Incidence in male prison populations was shown to be greatly increased compared to the general population. |
|
Definition
|
|
Term
Describe the behavioral problems associated with 47,XYY syndrome |
|
Definition
hyperactivity, ADD, learning disabilities, no evidence for inclination to commit violent crimes |
|
|
Term
About 1/__ pregnancies are lost after implantation. |
|
Definition
|
|
Term
What is the leading known cause of pregnancy loss? |
|
Definition
|
|
Term
A minimum of __% to __% of conceptions have a chromosome abnormality. At least __% of these are lost before term. |
|
Definition
|
|
Term
Studies of miscarriages show that about 50% of the chromosome abnormalities are _________, 20% are _______, 15% are _________, and the remainder consist of ______ and ______. |
|
Definition
trisomies, monosomies, triploids, tetraploids and structural abnormalities |
|
|
Term
Trisomy __ is thought to be the most common trisomy at conception, but it is never seen in live births |
|
Definition
|
|
Term
Balanced structural abnormalities of chromosomes often do NOT produce... |
|
Definition
serious health consequences |
|
|
Term
Alterations of chromosome structure can occur when chromosomes ___________ improperly during meiosis, or ________ during mitosis or meiosis. |
|
Definition
|
|
Term
What is the term for an agent that increases the likelihood of chromosome breakage? |
|
Definition
|
|
Term
The interchange of genetic material between nonhomologous chromosomes is called... |
|
Definition
|
|
Term
What are the two main types of translocations? |
|
Definition
Reciprocal and Robertsonian |
|
|
Term
The chromosome that results after a translocation involving equal exchange is called a... |
|
Definition
|
|
Term
What consequence is a reciprocal translocation to the carrier? What about to the offspring? |
|
Definition
Carrier is usually normal, offspring can be normal, carry the translocation or have duplications or deletions |
|
|
Term
What happens during a Robertsonian translocation? |
|
Definition
The short arms of two nonhomologous chromosomes are lost and the long arms fuse at the centromere. |
|
|
Term
Robertsonian translocation is confined to which chromosomes? Why? |
|
Definition
13, 14, 15, 21, and 22 - they are acrocentric and have very small short arms with no essential genes |
|
|
Term
Carriers of a Robertsonian translocation are phenotypically normal but have only ___ chromosomes in each cell. |
|
Definition
|
|
Term
A Robertsonian translocation can involve the fusion of the long arms of chromosomes 21 and 14. What would the karyotype of a male carrier be? |
|
Definition
|
|
Term
Carriers of a Robertsonian translocation can have what two types of segregation during gametogenesis? |
|
Definition
alternate or adjacent segregation |
|
|
Term
If alternate segregation occurs during gametogenesis, what is the consequence to the offspring? |
|
Definition
Either chromosomally normal or have a balanced translocation with normal phenotype |
|
|
Term
If adjacent segregation occurs during gametogenesis, what is the consequence to the offspring? |
|
Definition
offspring have have trisomy or monosomy of either chromosome involved in the translocation |
|
|
Term
Robertsonian translocations are responsible for approx __% of ______ syndrome cases. |
|
Definition
|
|
Term
Why should a karyotype be done on a child who has Down syndrome with 100% certainly based on clinical presentation? |
|
Definition
Recurrence risk for Down syndrome from Robertsonian translocation is greater than the non-disjunction type of Down syndrome, but the phenotype is the same |
|
|
Term
A break leading to the loss of a chromosome's tip is called a ... |
|
Definition
|
|
Term
When two breaks occur in a chromosome and the material between them is lost, it is called a.... |
|
Definition
|
|
Term
Which syndrome is caused by a deletion of the distal short arm of chromosome 5 (46,XY,del[5p])? |
|
Definition
|
|
Term
Cri-du-chat is seen in approx 1/_____ live births, and is characterized by... |
|
Definition
50,000, mental retardation, microcephaly, characteristic facial appearance |
|
|
Term
What causes Wolf-Hirschhorn syndrome? |
|
Definition
Deletion of the distal short arm of chromosome 4 |
|
|
Term
75% of Prader-Willi syndrome cases are caused by a microdeletion of which arm of which chromosome? |
|
Definition
|
|
Term
Microdeletion of paternal 15q results in ________, and of materal 15q results in _________. |
|
Definition
Prader-Willi syndrome, Angelman syndrome |
|
|
Term
WAGR syndrome can be produced by a deletion of 11p, and produces what main 4 features? |
|
Definition
Wilms tumor, aniridia, GU abnormalities, mental retardation |
|
|
Term
When a structural defect involving a series of adjacent genes produces a particular syndrome, it is called a __________ syndrome. |
|
Definition
|
|
Term
Which syndrome is characterized by mental retardation, supravalvular aortic stenosis, multiple peripheral pulmonary arterial stenosis, chacteristic facial features, dental malformations and hypercalcemia? What type of syndrome is it? |
|
Definition
Williams, a microdeletion syndrome |
|
|
Term
Which gene is located in the Williams syndrome critical region and is expressed in blood vessels? |
|
Definition
|
|
Term
Which gene in the critical region is likely to be involved in the visual-spatial cognition defects in Williams syndrome patients? |
|
Definition
|
|
Term
Deletion syndromes may be caused by multiple repeated sequences at the deletion boundaries, which promote... |
|
Definition
unequal crossing over, which then produces deletions |
|
|
Term
A condition in which one parent has contributes two copies of a chromosome and the other parent has contributed no copies is called... |
|
Definition
|
|
Term
What is it called when one parent contributes two copies of one homolog to the offspring? |
|
Definition
|
|
Term
What is it called when one parent contributes one copy of each homolog of a chromosome to the offspring? |
|
Definition
|
|
Term
What are the two main mechanisms by which a uniparental disomy may arise? |
|
Definition
trisomic conception followed by loss of one of the extra chromosomes, monosomic conception followed by mitotic nondisjunction |
|
|
Term
Uniparental disomy has been observed mainly in which syndromes? |
|
Definition
cystic fibrosis, Prader-Willi and Angelman, Beckwith-Wiedemann |
|
|
Term
What are the two main mechanisms by which duplications arise? |
|
Definition
Unequal crossover or from reciprocal translocation in the parent |
|
|
Term
How does a ring chromosome happen? |
|
Definition
Deletions at both tips of the chromosome, fusing of the ends |
|
|
Term
Ring chromosomes are often _____, resulting in _________ in at least some cells. |
|
Definition
|
|
Term
A chromosomal inversion is the result of... |
|
Definition
two breaks followed by reinsertion of the segment in an inverted order |
|
|
Term
What are the two main types of inversions? |
|
Definition
pericentric and paracentric |
|
|
Term
What is the consequence of an inversion for the carrier? The offspring? |
|
Definition
Seldom produce disease in the carrier, can produce abnormalities in offspring - often have deletions or duplications |
|
|
Term
It is estimated that about 1/____ people carries an inversion. |
|
Definition
|
|
Term
What results when a chromosome divides along an axis perpendicular to its usual axis of division? |
|
Definition
|
|
Term
What is different about an isochromosome? |
|
Definition
it has two copies of one arm of a chromosome and no copies of the other arm |
|
|
Term
Most isochromosomes observed in live births involve the __ chromosome. |
|
Definition
|
|
Term
A pericentric inversion causes the formation of a _____ during the alignment of homologous chromosomes in meiosis. |
|
Definition
|
|
Term
46,X,i[Xq] individuals usually have features of ________ syndrome. |
|
Definition
|
|
Term
What are the 4 main features that most chromosome abnormalities will display? |
|
Definition
developmental delay or mental retardation, facial morphogenic alteration, growth delay, congenital malformations |
|
|
Term
What are the most common clinical indications for chromosome analysis in the newborn? In the child? |
|
Definition
multiple congenital malformations, developmental retardation |
|
|
Term
CML commonly involves what chromosomal abnormality? What is the resultant chromosome called? |
|
Definition
Reciprocal translocation between chromosomes 9 and 22, Philadelphia chromosome |
|
|
Term
What is the mechanism by which the CML chromosome abnormality produces a defective gene? |
|
Definition
proto-oncogene abl is moved from 9q to 22q, alters the protein product, exhibits increased tyrosine kinase activity |
|
|
Term
What type of cancer is common in Africa and is associated with a translocation? What is the translocation? What effect does it have? |
|
Definition
Burkitt lymphoma, reciprocal translocation involving 8 and 14, moves myc proto-oncogene near the IG heavy chain loci, causes activation of myc |
|
|
Term
Some autosomal recessive diseases cause increased incidences of chromosome breaks, these are called _______________ syndromes. |
|
Definition
chromosome instability syndromes |
|
|
Term
Name several chromosome instability syndromes |
|
Definition
ataxia-telangiectasia, Bloom syndrome, Fanconi anemia, xeroderma pigmentosa |
|
|
Term
The chromosomal instability syndromes are associated with increased _________ risk. |
|
Definition
|
|