Mendelian Disorders
Important Questions on Mendelian Disorders
Describe the individuals having chromosomal abnormalities XO.
Why is it said that marriages between close relatives are fraught with danger for the next generation?
Define aneuploidy. How is it different from polyploidy? Describe the individuals having trisomy of the 21st chromosome.
Given alongside is the representation of a relevant part of amino acid composition of the p-chain of haemoglobin, related to the shape of human red blood cells.
Why is the disease referred to as a Mendelian disorder? Explain.
Name a genetic disorder where a human female is always a carrier yet rarely suffers from the disorder. Explain.
Why are 'colour blindness' and 'thalassemia' categorised as Mendelian disorders?
What is the karyotype of Turner’s syndrome?
Write the chromosomal defect in individuals affected with Klinefelter’s syndrome.
A disease which causes the black color of the urine
Phenylketonuria (PKU) is an inherited disease that refers to
The genetic defect - Adenosine deaminase (ADA) deficiency may be cured permanently by :
The recessive genes located on X-chromosome in humans are always
