263281
Phenylketonuria, sickle cell anemia and cystic fibrosis are caused respectively due to
1 Chromosome 7, Chromosome 11, Chromosome 12
2 Chromosome 12, Chromosome 11, Chromosome 7
3 Chromosome 11, Chromosome 18, Chromosome 9
4 Chromosome 18, Chromosome 11, Chromosome 9
Explanation:
B phenylketonuria is an autosomal recessive genetic disorder caused by mutation in the PAH gene, which is located on chromosome 12. This gene provides instruction for making an enzyme called phenylalanine hydroxylase. - Sickle cell anemia is caused by a mutation in the HBB gene, which is located on chromosome 11, this gene making a protein called hemoglobin. - Cystic fibrosis disorder is caused by mutation in the CFTR gene which is located on chromosome 7. It affects the lung and digestive system.
Shift-I
Human Health and Disease
263282
Kwashiorkor and beri-beri are:
1 communicable diseases
2 infectious diseases
3 deficiency diseases
4 none of the above
Explanation:
C Kwashiorkor and Beri-Beri both are deficiency disease which occur generally in children. Kwashiorkar occurs due to deficiency of protein and Beri-Beri due to deficiency of vitamin \(\mathrm{B}_{1}\) (Thiamin).
AFMC-2005
Human Health and Disease
263283
Tay Sach's disease is due to
1 sex linked recessive gene
2 sex linked dominant gene
3 autosomal dominant gene
4 autosomal recessive gene
Explanation:
D Tay sach's disease is inherited as an autosomal recessive disease. It is caused by genetic mutation in the HEXA gene on chromosome 15 which codes for hexosaminidase (an enzyme which serves in lipid metabolism.)
MGIMS Wardha-2007
Human Health and Disease
263284
Leprosy is also called as
1 Hansen's disease
2 sarcoma
3 slim disease
4 leukemia
Explanation:
A Hanseniasis or HD, Hansen's disease is also known as leprosy, it is an infection caused by slowgrowing bacteria called Mycobacterium leprae. This disease affects the skin, peripheral nerves, mucosal surface of respiratory tract. Rifampicin, the most important anti-leprosy medicine.
263281
Phenylketonuria, sickle cell anemia and cystic fibrosis are caused respectively due to
1 Chromosome 7, Chromosome 11, Chromosome 12
2 Chromosome 12, Chromosome 11, Chromosome 7
3 Chromosome 11, Chromosome 18, Chromosome 9
4 Chromosome 18, Chromosome 11, Chromosome 9
Explanation:
B phenylketonuria is an autosomal recessive genetic disorder caused by mutation in the PAH gene, which is located on chromosome 12. This gene provides instruction for making an enzyme called phenylalanine hydroxylase. - Sickle cell anemia is caused by a mutation in the HBB gene, which is located on chromosome 11, this gene making a protein called hemoglobin. - Cystic fibrosis disorder is caused by mutation in the CFTR gene which is located on chromosome 7. It affects the lung and digestive system.
Shift-I
Human Health and Disease
263282
Kwashiorkor and beri-beri are:
1 communicable diseases
2 infectious diseases
3 deficiency diseases
4 none of the above
Explanation:
C Kwashiorkor and Beri-Beri both are deficiency disease which occur generally in children. Kwashiorkar occurs due to deficiency of protein and Beri-Beri due to deficiency of vitamin \(\mathrm{B}_{1}\) (Thiamin).
AFMC-2005
Human Health and Disease
263283
Tay Sach's disease is due to
1 sex linked recessive gene
2 sex linked dominant gene
3 autosomal dominant gene
4 autosomal recessive gene
Explanation:
D Tay sach's disease is inherited as an autosomal recessive disease. It is caused by genetic mutation in the HEXA gene on chromosome 15 which codes for hexosaminidase (an enzyme which serves in lipid metabolism.)
MGIMS Wardha-2007
Human Health and Disease
263284
Leprosy is also called as
1 Hansen's disease
2 sarcoma
3 slim disease
4 leukemia
Explanation:
A Hanseniasis or HD, Hansen's disease is also known as leprosy, it is an infection caused by slowgrowing bacteria called Mycobacterium leprae. This disease affects the skin, peripheral nerves, mucosal surface of respiratory tract. Rifampicin, the most important anti-leprosy medicine.
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Human Health and Disease
263281
Phenylketonuria, sickle cell anemia and cystic fibrosis are caused respectively due to
1 Chromosome 7, Chromosome 11, Chromosome 12
2 Chromosome 12, Chromosome 11, Chromosome 7
3 Chromosome 11, Chromosome 18, Chromosome 9
4 Chromosome 18, Chromosome 11, Chromosome 9
Explanation:
B phenylketonuria is an autosomal recessive genetic disorder caused by mutation in the PAH gene, which is located on chromosome 12. This gene provides instruction for making an enzyme called phenylalanine hydroxylase. - Sickle cell anemia is caused by a mutation in the HBB gene, which is located on chromosome 11, this gene making a protein called hemoglobin. - Cystic fibrosis disorder is caused by mutation in the CFTR gene which is located on chromosome 7. It affects the lung and digestive system.
Shift-I
Human Health and Disease
263282
Kwashiorkor and beri-beri are:
1 communicable diseases
2 infectious diseases
3 deficiency diseases
4 none of the above
Explanation:
C Kwashiorkor and Beri-Beri both are deficiency disease which occur generally in children. Kwashiorkar occurs due to deficiency of protein and Beri-Beri due to deficiency of vitamin \(\mathrm{B}_{1}\) (Thiamin).
AFMC-2005
Human Health and Disease
263283
Tay Sach's disease is due to
1 sex linked recessive gene
2 sex linked dominant gene
3 autosomal dominant gene
4 autosomal recessive gene
Explanation:
D Tay sach's disease is inherited as an autosomal recessive disease. It is caused by genetic mutation in the HEXA gene on chromosome 15 which codes for hexosaminidase (an enzyme which serves in lipid metabolism.)
MGIMS Wardha-2007
Human Health and Disease
263284
Leprosy is also called as
1 Hansen's disease
2 sarcoma
3 slim disease
4 leukemia
Explanation:
A Hanseniasis or HD, Hansen's disease is also known as leprosy, it is an infection caused by slowgrowing bacteria called Mycobacterium leprae. This disease affects the skin, peripheral nerves, mucosal surface of respiratory tract. Rifampicin, the most important anti-leprosy medicine.
263281
Phenylketonuria, sickle cell anemia and cystic fibrosis are caused respectively due to
1 Chromosome 7, Chromosome 11, Chromosome 12
2 Chromosome 12, Chromosome 11, Chromosome 7
3 Chromosome 11, Chromosome 18, Chromosome 9
4 Chromosome 18, Chromosome 11, Chromosome 9
Explanation:
B phenylketonuria is an autosomal recessive genetic disorder caused by mutation in the PAH gene, which is located on chromosome 12. This gene provides instruction for making an enzyme called phenylalanine hydroxylase. - Sickle cell anemia is caused by a mutation in the HBB gene, which is located on chromosome 11, this gene making a protein called hemoglobin. - Cystic fibrosis disorder is caused by mutation in the CFTR gene which is located on chromosome 7. It affects the lung and digestive system.
Shift-I
Human Health and Disease
263282
Kwashiorkor and beri-beri are:
1 communicable diseases
2 infectious diseases
3 deficiency diseases
4 none of the above
Explanation:
C Kwashiorkor and Beri-Beri both are deficiency disease which occur generally in children. Kwashiorkar occurs due to deficiency of protein and Beri-Beri due to deficiency of vitamin \(\mathrm{B}_{1}\) (Thiamin).
AFMC-2005
Human Health and Disease
263283
Tay Sach's disease is due to
1 sex linked recessive gene
2 sex linked dominant gene
3 autosomal dominant gene
4 autosomal recessive gene
Explanation:
D Tay sach's disease is inherited as an autosomal recessive disease. It is caused by genetic mutation in the HEXA gene on chromosome 15 which codes for hexosaminidase (an enzyme which serves in lipid metabolism.)
MGIMS Wardha-2007
Human Health and Disease
263284
Leprosy is also called as
1 Hansen's disease
2 sarcoma
3 slim disease
4 leukemia
Explanation:
A Hanseniasis or HD, Hansen's disease is also known as leprosy, it is an infection caused by slowgrowing bacteria called Mycobacterium leprae. This disease affects the skin, peripheral nerves, mucosal surface of respiratory tract. Rifampicin, the most important anti-leprosy medicine.
263281
Phenylketonuria, sickle cell anemia and cystic fibrosis are caused respectively due to
1 Chromosome 7, Chromosome 11, Chromosome 12
2 Chromosome 12, Chromosome 11, Chromosome 7
3 Chromosome 11, Chromosome 18, Chromosome 9
4 Chromosome 18, Chromosome 11, Chromosome 9
Explanation:
B phenylketonuria is an autosomal recessive genetic disorder caused by mutation in the PAH gene, which is located on chromosome 12. This gene provides instruction for making an enzyme called phenylalanine hydroxylase. - Sickle cell anemia is caused by a mutation in the HBB gene, which is located on chromosome 11, this gene making a protein called hemoglobin. - Cystic fibrosis disorder is caused by mutation in the CFTR gene which is located on chromosome 7. It affects the lung and digestive system.
Shift-I
Human Health and Disease
263282
Kwashiorkor and beri-beri are:
1 communicable diseases
2 infectious diseases
3 deficiency diseases
4 none of the above
Explanation:
C Kwashiorkor and Beri-Beri both are deficiency disease which occur generally in children. Kwashiorkar occurs due to deficiency of protein and Beri-Beri due to deficiency of vitamin \(\mathrm{B}_{1}\) (Thiamin).
AFMC-2005
Human Health and Disease
263283
Tay Sach's disease is due to
1 sex linked recessive gene
2 sex linked dominant gene
3 autosomal dominant gene
4 autosomal recessive gene
Explanation:
D Tay sach's disease is inherited as an autosomal recessive disease. It is caused by genetic mutation in the HEXA gene on chromosome 15 which codes for hexosaminidase (an enzyme which serves in lipid metabolism.)
MGIMS Wardha-2007
Human Health and Disease
263284
Leprosy is also called as
1 Hansen's disease
2 sarcoma
3 slim disease
4 leukemia
Explanation:
A Hanseniasis or HD, Hansen's disease is also known as leprosy, it is an infection caused by slowgrowing bacteria called Mycobacterium leprae. This disease affects the skin, peripheral nerves, mucosal surface of respiratory tract. Rifampicin, the most important anti-leprosy medicine.