Give scientific reasons : The product of phenylalanine catabolism excreted in the urine in phenylketonuria.
It is a rare disease in which individual lacks an enzyme called Phenylalanine hydroxylase. Which is needed to breakdown an essential amino acid phenylalanine into tyrosine in liver. This phenylalanine is accumulated and gets converted into phenylpyruvic acid and other derivatives
leading to mental retardation (due to accumulation in brain). These are also excreted through urine because of its poor absorption by kidney.
Given below is a pedigree chart showing the inheritance of a certain sex- linked trait in humans.
The trait traced in the above pedigree chart is
What is the cause of haemophilia
Give differences : Haemophilia and Sickle-cell Anaemia
Which of these is not a Mendelian disorder?