Give differences : Haemophilia and Sickle-cel | vedclass

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Haemophilia
			Sickle-cell Anaemia
		
		
			$(1)$ It occur due to a defective recessive allele present on the $X$-chromosome.
			$(1)

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Haemophilia
			Sickle-cell Anaemia
		
		
			$(1)$ It occur due to a defective recessive allele present on the $X$-chromosome.
			$(1)$ It occurs due to point mutation i.e. a single base pair change leads to a change in amino acid.
		
		
			$(2)$ The defective allele produce nonfunctional protein which later form a non-functional protein which later form a non-functional cascade of protein involving in blood clotting
			$(2)$ In this glutamic ($Glu$) acid is replaced by Valine ($Val$) at sixth position of beta globin chain of haemoglobin molecule.
		
		
			$(3)$ It is a sex-linked recessive disorder.
			$(3)$ It is an autosomal linked recessive disorder.
		
		
			$(4)$ More males are affected than females.
			$(4)$ Both males and females are affected equally.

Column $I$	Column $II$
$(a)$ Sickle cell anaemia	$(x)$ Homogentisic acid
$(b)$ Alkaptonuria	$(y)$ Melanin pigmentsare absent
$(c)$ Albinism	$(z)$ More amount of phenyl alanine
$(d)$ Phenyl Ketonuria	$(w)$ Defective haemoglobin

Give differences : Haemophilia and Sickle-cell Anaemia

Similar Questions

:Match the columns :

Column $I$
Column $II$

$(a)$ Sickle cell anaemia $(x)$ Homogentisic acid

$(b)$ Alkaptonuria $(y)$ Melanin pigmentsare absent

$(c)$ Albinism $(z)$ More amount of phenyl alanine

$(d)$ Phenyl Ketonuria $(w)$ Defective haemoglobin

Sex linked disease is

Sickle cell anaemia is due to

Given below is a highly simplified representation of the human sex chromosomes from a karyotype. The gene $'a'$ and $'b'$ could be of

If a character is always transmitted directly from a father to all his sons and from their sons to all their sons, then which chromosome carries the gene for the character

Haemophilia	Sickle-cell Anaemia
$(1)$ It occur due to a defective recessive allele present on the $X$-chromosome.	$(1)$ It occurs due to point mutation i.e. a single base pair change leads to a change in amino acid.
$(2)$ The defective allele produce nonfunctional protein which later form a non-functional protein which later form a non-functional cascade of protein involving in blood clotting	$(2)$ In this glutamic ($Glu$) acid is replaced by Valine ($Val$) at sixth position of beta globin chain of haemoglobin molecule.
$(3)$ It is a sex-linked recessive disorder.	$(3)$ It is an autosomal linked recessive disorder.
$(4)$ More males are affected than females.	$(4)$ Both males and females are affected equally.