184776
Which one of the following can help in the diagnosis of genetical disorder?
1 ELISA
2 ABO blood group
3 \(\mathbf{P C R}\)
4 NMR
Explanation:
: PCR (Polymerase chain reaction) is a technique used to amplify a single copy or few copies of a piece of DNA to produce multiple copies of the same sequence PCR can be used as a diagnostic tool, where a sample of DNA is analyzed for the presence of genetic irsease che to mutations.
CMC Vellore-2012
Principle of Inheritance and Variation
184778
If a colour blind man marries a woman who is normal but carries this trait, the progeny will be:
1 all normal females but carrier of the trait
2 all males and \(50 \%\) females colour blind
3 all females and \(50 \%\) males colour blind
4 \(50 \%\) males and \(50 \%\) females colour blind
Explanation:
MP PMT-2013
Principle of Inheritance and Variation
184779
Gauchers disease is genetic disorder, which is associated with the abnormal metabolism of
1 glucose
2 fat
3 protein
4 All of the above
Explanation:
: Gaucher's disease is named after the French doctor Philippe Gaucher (1854 - 1918) who originally described it in 1882. Gaucher's disease is a genetic disease associsted with abromal fat metabolism, caused by the absence of the enzyme glucocerebrosidase requited for proper processing of lipids. Non-processing of lipid results in accumulation of fatty material in spleen liver, bone marrow and brain. The swelling of these organs occurs and patients usually cie by the age of 15 years.
BVP-2014
Principle of Inheritance and Variation
184780
Hurlers disease is caused by
1 presence of amino acid tyrosine
2 presence of lysosomes
3 absence of lysosomes
4 absence of amino acid tyrosine
Explanation:
: Hurler's cisease is named after a German pediatrician Gertud Hurler. It is caused by the deficiency of lysosomes which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This tinally results in the accumulation of large amount of GAG in the body, eventually causing the cells to become severely dysfimctional leading to death.
BVP-2014
Principle of Inheritance and Variation
184785
Genetic disorder hemophilia is characterized by excessive loss of blood. Which of the following statements is not true in relation to this disease?
1 It is an autosomal disease
2 It is a X-linked disease
3 Any of the factor VIII of IX may be absent
4 It is a lethal clisease
Explanation:
: Haemophilia is X-linked recessive clisease. It is caused due to the lack of factor VIII (antihaemophillic globulin) and factor IX (Plasma Thromboplastic Component or PTC). It is characterized by free bleeding from even slight wound because of the lack of formation of clotting factors therefore it is called as lethal disease as it may cause death if the bleecing cantrot be stopped or if it occurs in a vital organ such as the brain.
184776
Which one of the following can help in the diagnosis of genetical disorder?
1 ELISA
2 ABO blood group
3 \(\mathbf{P C R}\)
4 NMR
Explanation:
: PCR (Polymerase chain reaction) is a technique used to amplify a single copy or few copies of a piece of DNA to produce multiple copies of the same sequence PCR can be used as a diagnostic tool, where a sample of DNA is analyzed for the presence of genetic irsease che to mutations.
CMC Vellore-2012
Principle of Inheritance and Variation
184778
If a colour blind man marries a woman who is normal but carries this trait, the progeny will be:
1 all normal females but carrier of the trait
2 all males and \(50 \%\) females colour blind
3 all females and \(50 \%\) males colour blind
4 \(50 \%\) males and \(50 \%\) females colour blind
Explanation:
MP PMT-2013
Principle of Inheritance and Variation
184779
Gauchers disease is genetic disorder, which is associated with the abnormal metabolism of
1 glucose
2 fat
3 protein
4 All of the above
Explanation:
: Gaucher's disease is named after the French doctor Philippe Gaucher (1854 - 1918) who originally described it in 1882. Gaucher's disease is a genetic disease associsted with abromal fat metabolism, caused by the absence of the enzyme glucocerebrosidase requited for proper processing of lipids. Non-processing of lipid results in accumulation of fatty material in spleen liver, bone marrow and brain. The swelling of these organs occurs and patients usually cie by the age of 15 years.
BVP-2014
Principle of Inheritance and Variation
184780
Hurlers disease is caused by
1 presence of amino acid tyrosine
2 presence of lysosomes
3 absence of lysosomes
4 absence of amino acid tyrosine
Explanation:
: Hurler's cisease is named after a German pediatrician Gertud Hurler. It is caused by the deficiency of lysosomes which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This tinally results in the accumulation of large amount of GAG in the body, eventually causing the cells to become severely dysfimctional leading to death.
BVP-2014
Principle of Inheritance and Variation
184785
Genetic disorder hemophilia is characterized by excessive loss of blood. Which of the following statements is not true in relation to this disease?
1 It is an autosomal disease
2 It is a X-linked disease
3 Any of the factor VIII of IX may be absent
4 It is a lethal clisease
Explanation:
: Haemophilia is X-linked recessive clisease. It is caused due to the lack of factor VIII (antihaemophillic globulin) and factor IX (Plasma Thromboplastic Component or PTC). It is characterized by free bleeding from even slight wound because of the lack of formation of clotting factors therefore it is called as lethal disease as it may cause death if the bleecing cantrot be stopped or if it occurs in a vital organ such as the brain.
184776
Which one of the following can help in the diagnosis of genetical disorder?
1 ELISA
2 ABO blood group
3 \(\mathbf{P C R}\)
4 NMR
Explanation:
: PCR (Polymerase chain reaction) is a technique used to amplify a single copy or few copies of a piece of DNA to produce multiple copies of the same sequence PCR can be used as a diagnostic tool, where a sample of DNA is analyzed for the presence of genetic irsease che to mutations.
CMC Vellore-2012
Principle of Inheritance and Variation
184778
If a colour blind man marries a woman who is normal but carries this trait, the progeny will be:
1 all normal females but carrier of the trait
2 all males and \(50 \%\) females colour blind
3 all females and \(50 \%\) males colour blind
4 \(50 \%\) males and \(50 \%\) females colour blind
Explanation:
MP PMT-2013
Principle of Inheritance and Variation
184779
Gauchers disease is genetic disorder, which is associated with the abnormal metabolism of
1 glucose
2 fat
3 protein
4 All of the above
Explanation:
: Gaucher's disease is named after the French doctor Philippe Gaucher (1854 - 1918) who originally described it in 1882. Gaucher's disease is a genetic disease associsted with abromal fat metabolism, caused by the absence of the enzyme glucocerebrosidase requited for proper processing of lipids. Non-processing of lipid results in accumulation of fatty material in spleen liver, bone marrow and brain. The swelling of these organs occurs and patients usually cie by the age of 15 years.
BVP-2014
Principle of Inheritance and Variation
184780
Hurlers disease is caused by
1 presence of amino acid tyrosine
2 presence of lysosomes
3 absence of lysosomes
4 absence of amino acid tyrosine
Explanation:
: Hurler's cisease is named after a German pediatrician Gertud Hurler. It is caused by the deficiency of lysosomes which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This tinally results in the accumulation of large amount of GAG in the body, eventually causing the cells to become severely dysfimctional leading to death.
BVP-2014
Principle of Inheritance and Variation
184785
Genetic disorder hemophilia is characterized by excessive loss of blood. Which of the following statements is not true in relation to this disease?
1 It is an autosomal disease
2 It is a X-linked disease
3 Any of the factor VIII of IX may be absent
4 It is a lethal clisease
Explanation:
: Haemophilia is X-linked recessive clisease. It is caused due to the lack of factor VIII (antihaemophillic globulin) and factor IX (Plasma Thromboplastic Component or PTC). It is characterized by free bleeding from even slight wound because of the lack of formation of clotting factors therefore it is called as lethal disease as it may cause death if the bleecing cantrot be stopped or if it occurs in a vital organ such as the brain.
NEET Test Series from KOTA - 10 Papers In MS WORD
WhatsApp Here
Principle of Inheritance and Variation
184776
Which one of the following can help in the diagnosis of genetical disorder?
1 ELISA
2 ABO blood group
3 \(\mathbf{P C R}\)
4 NMR
Explanation:
: PCR (Polymerase chain reaction) is a technique used to amplify a single copy or few copies of a piece of DNA to produce multiple copies of the same sequence PCR can be used as a diagnostic tool, where a sample of DNA is analyzed for the presence of genetic irsease che to mutations.
CMC Vellore-2012
Principle of Inheritance and Variation
184778
If a colour blind man marries a woman who is normal but carries this trait, the progeny will be:
1 all normal females but carrier of the trait
2 all males and \(50 \%\) females colour blind
3 all females and \(50 \%\) males colour blind
4 \(50 \%\) males and \(50 \%\) females colour blind
Explanation:
MP PMT-2013
Principle of Inheritance and Variation
184779
Gauchers disease is genetic disorder, which is associated with the abnormal metabolism of
1 glucose
2 fat
3 protein
4 All of the above
Explanation:
: Gaucher's disease is named after the French doctor Philippe Gaucher (1854 - 1918) who originally described it in 1882. Gaucher's disease is a genetic disease associsted with abromal fat metabolism, caused by the absence of the enzyme glucocerebrosidase requited for proper processing of lipids. Non-processing of lipid results in accumulation of fatty material in spleen liver, bone marrow and brain. The swelling of these organs occurs and patients usually cie by the age of 15 years.
BVP-2014
Principle of Inheritance and Variation
184780
Hurlers disease is caused by
1 presence of amino acid tyrosine
2 presence of lysosomes
3 absence of lysosomes
4 absence of amino acid tyrosine
Explanation:
: Hurler's cisease is named after a German pediatrician Gertud Hurler. It is caused by the deficiency of lysosomes which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This tinally results in the accumulation of large amount of GAG in the body, eventually causing the cells to become severely dysfimctional leading to death.
BVP-2014
Principle of Inheritance and Variation
184785
Genetic disorder hemophilia is characterized by excessive loss of blood. Which of the following statements is not true in relation to this disease?
1 It is an autosomal disease
2 It is a X-linked disease
3 Any of the factor VIII of IX may be absent
4 It is a lethal clisease
Explanation:
: Haemophilia is X-linked recessive clisease. It is caused due to the lack of factor VIII (antihaemophillic globulin) and factor IX (Plasma Thromboplastic Component or PTC). It is characterized by free bleeding from even slight wound because of the lack of formation of clotting factors therefore it is called as lethal disease as it may cause death if the bleecing cantrot be stopped or if it occurs in a vital organ such as the brain.
184776
Which one of the following can help in the diagnosis of genetical disorder?
1 ELISA
2 ABO blood group
3 \(\mathbf{P C R}\)
4 NMR
Explanation:
: PCR (Polymerase chain reaction) is a technique used to amplify a single copy or few copies of a piece of DNA to produce multiple copies of the same sequence PCR can be used as a diagnostic tool, where a sample of DNA is analyzed for the presence of genetic irsease che to mutations.
CMC Vellore-2012
Principle of Inheritance and Variation
184778
If a colour blind man marries a woman who is normal but carries this trait, the progeny will be:
1 all normal females but carrier of the trait
2 all males and \(50 \%\) females colour blind
3 all females and \(50 \%\) males colour blind
4 \(50 \%\) males and \(50 \%\) females colour blind
Explanation:
MP PMT-2013
Principle of Inheritance and Variation
184779
Gauchers disease is genetic disorder, which is associated with the abnormal metabolism of
1 glucose
2 fat
3 protein
4 All of the above
Explanation:
: Gaucher's disease is named after the French doctor Philippe Gaucher (1854 - 1918) who originally described it in 1882. Gaucher's disease is a genetic disease associsted with abromal fat metabolism, caused by the absence of the enzyme glucocerebrosidase requited for proper processing of lipids. Non-processing of lipid results in accumulation of fatty material in spleen liver, bone marrow and brain. The swelling of these organs occurs and patients usually cie by the age of 15 years.
BVP-2014
Principle of Inheritance and Variation
184780
Hurlers disease is caused by
1 presence of amino acid tyrosine
2 presence of lysosomes
3 absence of lysosomes
4 absence of amino acid tyrosine
Explanation:
: Hurler's cisease is named after a German pediatrician Gertud Hurler. It is caused by the deficiency of lysosomes which aids in the breakdown of dermatan sulfate and heparin sulfate (GAG). This tinally results in the accumulation of large amount of GAG in the body, eventually causing the cells to become severely dysfimctional leading to death.
BVP-2014
Principle of Inheritance and Variation
184785
Genetic disorder hemophilia is characterized by excessive loss of blood. Which of the following statements is not true in relation to this disease?
1 It is an autosomal disease
2 It is a X-linked disease
3 Any of the factor VIII of IX may be absent
4 It is a lethal clisease
Explanation:
: Haemophilia is X-linked recessive clisease. It is caused due to the lack of factor VIII (antihaemophillic globulin) and factor IX (Plasma Thromboplastic Component or PTC). It is characterized by free bleeding from even slight wound because of the lack of formation of clotting factors therefore it is called as lethal disease as it may cause death if the bleecing cantrot be stopped or if it occurs in a vital organ such as the brain.
