Question
Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue. The symptoms of this disorder range from skeletal issues to problems with the nervous and cardiovascular systems. This is an example of

Question 17 2.1 pts Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answer :

PLEIOTROPY.

Discussion and explanation :

Pleiotropy is a phenomenon when one gene controls or effects many phenotypic characters.

When a single phenotype (skin colour) is controlled by multiple genes, this genetic phenomenon is termed as polygenic inheritance.

Epistasis is a phenomenon in which one gene (modifier gene) effects the expression of another unrelated gene or allele.

When two or more alleles of a single gene get expressed completely as in ABO blood groups, the phenomenon is termed as codominance.

Linkage is the phenomenon in which two closely located genes are inherited together during meiosis in gamete formation.

Marfan syndrome is an autosomal dominant connective tissue disorder due to mutation in Fibrillin gene on chromosome 15. This single gene mutation effects many systems as given below :

1) Skeletal changes - Tall stature, long fingers (arachnodactyly), chest deformity (such as pectus exacavatum).

2) Ocular changes - Dislocation of lens (ectopia lentis), risk of retinal detachment.

3) Cardiovascular changes - Dilated aorta, aortic regurgitation, mitral valve prolapse.

Thus, Marfan syndrome is example of pleiotropy.

Add a comment
Know the answer?
Add Answer to:
Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue....
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Marfan Syndrome, one of the most common inherited disorders of connective tissue, is caused by an...

    Marfan Syndrome, one of the most common inherited disorders of connective tissue, is caused by an autosomal dominant mutation within the fibrillin-1 gene (FBN1) on the short arm of chromosome 15. Pooled ten-year records from several large hospitals in the United States revealed that, among 5,000,000 live births (=10,000,000 gametes), the total number of babies born with Marfan Syndrome was 250. Among those 250 babies, 187 of them had at least one parent with Marfan Syndrome, and the remaining babies...

  • Suppose there is a genetic disorder caused by a single base change in a gene on...

    Suppose there is a genetic disorder caused by a single base change in a gene on chromosome 11, which changes a cellular protein so that its function is altered. This mutation happens also to eliminate a cleavage site for a restriction endonuclease EcoRI (sequence: 5'-GAATTC-3'). If you isolated a portion of chromosome 11 DNA containing this defective gene, explain exactly how could you use restriction enzymes and gel electrophoresis to detect the base change. Please write 500 words or fewer.

  • Saved raph to describe how blood types are inherited in humans. When a trait is controlled...

    Saved raph to describe how blood types are inherited in humans. When a trait is controlled by forms. alleles, the gene exists in several allelic However, each individual will still only possess of the possible alleles. For example, ABO blood types. alleles for the same gene control the inheritance of These alleles determine the presence or absence of cells. on red blood The allele encodes for the production of antigen, the allele encodes for antigen production and the i allele...

  • TOPIC #2: LEIGH'S SYNDROME - CELLULAR RESPIRATION AND HEALTH Cellular respiration is vital to our health....

    TOPIC #2: LEIGH'S SYNDROME - CELLULAR RESPIRATION AND HEALTH Cellular respiration is vital to our health. When it fails to work properly, serious diseases (and even death) occur. The connections between disease and respiration (glycolysis, the intermediate step, citric acid cycle (i.e. Krebs cycle), and the electron transport chain (ETC) are being studied by scientists. While many mysteries still remain, much is also known. Leigh's syndrome is a rare central nervous system degenerative disorder that is due to various problems...

  • Case: Genetic Disorder of GLUT 1 Deficiency Syndrome Background: Nadia, a 6-year-old White female, has been...

    Case: Genetic Disorder of GLUT 1 Deficiency Syndrome Background: Nadia, a 6-year-old White female, has been to admitted to Children's National Hospital with parental c/o frequent episodes of seizures 1-2 times every other day for the past month. Parents report that she has been lethargic and having difficulty concentrating in school, and issues with age-appropriate articulation of speech, during this period. Prior to this admission, patient has been seen by her PCP as medical diagnosis remained undetermined. On admission, the...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT