.A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

.A disease caused by an autosomal primary non-
disjunction is
(a) Klinefelter’s syndrome
(b) Turner’s syndrome
(c) Sickle cell anaemia
(d) Down’s syndrome.
by

1 Answer

Answer :

(d) Down’s syndrome.
by

Related questions

A disease caused by an autosomal primary non- disjunction is : (1) Klinefelter's Syndrome(2) Turner's Syndrome (3) Sickel Cell Anemia (4) Down's Syndrome

Description : A disease caused by an autosomal primary non- disjunction is : (1) Klinefelter's Syndrome(2) Turner's Syndrome (3) Sickel Cell Anemia (4) Down's Syndrome

Last Answer : (4) Down's Syndrome

Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down’s syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X-linked recessive gene disorder. (a) (1), (3) and (4) are correct. (b) (1), (2) and (3) are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Description : Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down's syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X- ... are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Last Answer : (b) (1), (2) and (3) are correct.

Webbed neck is a characteristic of – (1) Down's syndrome (2) Turner's syndrome (3) Klinefelter's syndrome (4) Cri-du-chat syndrome

Description : Webbed neck is a characteristic of – (1) Down's syndrome (2) Turner's syndrome (3) Klinefelter's syndrome (4) Cri-du-chat syndrome

Last Answer : (2) Turner's syndrome Explanation: A webbed neck, or pterygium colli deformity, is a congenital skin fold that runs along the sides of the neck down to the shouldersit is a feature of Turner ... Syndrome (TS) is a condition in which a female is partly or completely missing an X chromosome.

.In which of the following diseases, the man has an extra X-chromosome? (a) Turner’s syndrome (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Haemophilia

Description : .In which of the following diseases, the man has an extra X-chromosome? (a) Turner’s syndrome (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Haemophilia

Last Answer : (b) Klinefelter’s syndrome

.A person with the sex chromosomes XXY suffers from (a) gynandromorphism (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Turner’s syndrome.

Description : .A person with the sex chromosomes XXY suffers from (a) gynandromorphism (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Turner’s syndrome.

Last Answer : (b) Klinefelter’s syndrome

Mongolian Idiocy due to trisomy in 21st chromsome is called (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Triple X syndrome

Description : Mongolian Idiocy due to trisomy in 21st chromsome is called (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Triple X syndrome

Last Answer : (a) Down’s syndrome

What is the genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile? (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Edward syndrome

Description : What is the genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile? (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Edward syndrome

Last Answer : Klinefelter’s syndrome

Webbed neck is a characteristic of (1) Down’s syndrome (2) Turner’s syndrome (3) Klinefelter’s syndrome (4) Cri–du–chat syndrome

Description : Webbed neck is a characteristic of (1) Down’s syndrome (2) Turner’s syndrome (3) Klinefelter’s syndrome (4) Cri–du–chat syndrome

Last Answer : Turner’s syndrome

Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Description : Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Last Answer : a) Down’s syndrome - 21st chromosome

The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Description : The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Last Answer : (b) sickle cell anaemia

. Sickle-cell anaemia is (a) caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin (b) caused by a change in a single base pair of DNA (c) characterized by elongated sickle like RBCs with a nucleus (d) an autosomal linked dominant trait.

Description : . Sickle-cell anaemia is (a) caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin (b) caused by a change in a single base pair of DNA (c) characterized by elongated sickle like RBCs with a nucleus (d) an autosomal linked dominant trait.

Last Answer : (b) caused by a change in a single base pair of DNA

Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait(c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Description : Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Last Answer : (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11

Down’s syndrome is due to (a) crossing over (b) linkage (c) sex-linked inheritance (d) non-disjunction of chromosomes.

Description : Down’s syndrome is due to (a) crossing over (b) linkage (c) sex-linked inheritance (d) non-disjunction of chromosomes.

Last Answer : (d) non-disjunction of chromosomes.

An abnormal human male phenotype involving an extra X-chromosome (XXY) is a case of (a) Edward’s syndrome (b) Klinefelter’s syndrome (c) intersex (d) Down’s syndrome.

Description : An abnormal human male phenotype involving an extra X-chromosome (XXY) is a case of (a) Edward’s syndrome (b) Klinefelter’s syndrome (c) intersex (d) Down’s syndrome.

Last Answer : (b) Klinefelter’s syndrome

.Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage? (a) Erythroblastosis fetalis - X-linked (b) Down’s syndrome - 44 autosomes + XO (c) Klinefelter’s syndrome - 44 autosomes + XXY (d) Colour blindness - Y-linked

Description : .Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage? (a) Erythroblastosis fetalis - X-linked (b) Down’s syndrome - 44 autosomes + XO (c) Klinefelter’s syndrome - 44 autosomes + XXY (d) Colour blindness - Y-linked

Last Answer : (c) Klinefelter’s syndrome - 44 autosomes + XXY

Which of the following cannot be detected in a developing fetus by amniocentesis? (a) Down’s syndrome (b) Jaundice (c) Klinefelter’s syndrome (d) Sex of the fetus

Description : Which of the following cannot be detected in a developing fetus by amniocentesis? (a) Down’s syndrome (b) Jaundice (c) Klinefelter’s syndrome (d) Sex of the fetus

Last Answer : (b) Jaundice

.In human beings 45 chromosomes/single X/XO abnormality causes (a) Down’s syndrome (b) Kinefelter’s syndrome (c) Turner’s syndrome (d) Edward’s syndrome

Description : .In human beings 45 chromosomes/single X/XO abnormality causes (a) Down’s syndrome (b) Kinefelter’s syndrome (c) Turner’s syndrome (d) Edward’s syndrome

Last Answer : (c) Turner’s syndrome

A woman with 47 chromosomes due to three copies of chromosome 21 is characterised by (a) superfemaleness (b) triploidy (c) Turner’s syndrome (d) Down’s syndrome.

Description : A woman with 47 chromosomes due to three copies of chromosome 21 is characterised by (a) superfemaleness (b) triploidy (c) Turner’s syndrome (d) Down’s syndrome.

Last Answer : (d) Down’s syndrome.

How is analyzing the inheritance patterns of sickle cell disease through pedigrees allowed scientists to determine that the disease is autosomal recessive?

Description : How is analyzing the inheritance patterns of sickle cell disease through pedigrees allowed scientists to determine that the disease is autosomal recessive?

Last Answer : Feel Free to Answer

Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Select the correct statement. (a) Both are due to a quantitative defect in globin chain synthesis. (b) Thalassemia is due to less synthesis of globin molecules. (c) Sickle cell anaemia is due to a quantitative problem of globin molecules. (d) Both are due to a qualitative defect in globin chain synthesis.

Description : Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Select the correct statement. (a) Both are due to a quantitative defect in globin chain synthesis. (b ... problem of globin molecules. (d) Both are due to a qualitative defect in globin chain synthesis.

Last Answer : (b) Thalassemia is due to less synthesis of globin molecules

.Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Description : .Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Last Answer : (b) Sickle cell anaemia

Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Description : Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Last Answer : (d) it provides immunity against malaria.

Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is one of the STDs.(c) Genital herpes and sickle-cell anaemia are both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Description : Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is ... both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Last Answer : (d) The chances of a 5-years boy contracting a STD are very little.

Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Description : Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Last Answer : causes retinal vein occlusion

A 28 year old patient complains of amenorrhea after having dilatation and curettage. The most likely diagnosis is: a) Kallman’s Syndrome. b) Turner’s Syndrome. c) Asherman’s Syndrome. d) Pelvic inflammatory disease. e) Anorexia nervosa.

Description : A 28 year old patient complains of amenorrhea after having dilatation and curettage. The most likely diagnosis is: a) Kallman’s Syndrome. b) Turner’s Syndrome. c) Asherman’s Syndrome. d) Pelvic inflammatory disease. e) Anorexia nervosa.

Last Answer : c) Asherman’s Syndrome.

Abnormal chain of amino acids in sickle cell anaemia is (A) Alpha chain (B) Beta chain (C) Delta chain (D) Gama chain

Description : Abnormal chain of amino acids in sickle cell anaemia is (A) Alpha chain (B) Beta chain (C) Delta chain (D) Gama chain

Last Answer : Answer : B

Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Description : Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Last Answer : (2) Leukaemia Explanation: Leukemia is a cancer of blood and bone marrow. When a person has leukemia, the body makes too many white blood cells (leukocytes). The causes of most types of leukemia are not known. In general, all cancers have a breakdown in the normal way cell division is controlled.

The oxygen dissociation curve is shifted to the right with: a. polycythaemia b. pyrexia c. respiratory acidosis d. sickle cell anaemia

Description : The oxygen dissociation curve is shifted to the right with: a. polycythaemia b. pyrexia c. respiratory acidosis d. sickle cell anaemia

Last Answer : pyrexia

Sickle cell anaemia induce to (a) change of amino acid in a-chain of haemoglobin (b) change of amino acid in b-chain of haemoglobin (c) change of amino acid in both a and b chains of haemoglobin (d) change of amino acid either a or b chains of haemoglobin.

Description : Sickle cell anaemia induce to (a) change of amino acid in a-chain of haemoglobin (b) change of amino acid in b-chain of haemoglobin (c) change of amino acid in both a and b chains of haemoglobin (d) change of amino acid either a or b chains of haemoglobin.

Last Answer : (b) change of amino acid in b-chain of haemoglobin

Both sickle cell anaemia and Huntington’s chorea are (a) virus-related diseases (b) bacteria-related diseases (c) congenital disorders (d) pollutant-induced disorders.

Description : Both sickle cell anaemia and Huntington’s chorea are (a) virus-related diseases (b) bacteria-related diseases (c) congenital disorders (d) pollutant-induced disorders.

Last Answer : c) congenital disorders

.Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Description : .Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Last Answer : (c) Haemophilia

Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Description : Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Last Answer : (c) Sickle cell anaemia

A polygenic inheritance in human beings is (a) skin colour (b) phenylketonuria (c) colour blindness (d) sickle cell anaemia

Description : A polygenic inheritance in human beings is (a) skin colour (b) phenylketonuria (c) colour blindness (d) sickle cell anaemia

Last Answer : (a) skin colour

In human beings, multiple genes are involved in the inheritance of (a) sickle-cell anaemia (b) skin colour (c) colour blindness (d) phenylketonuria.

Description : In human beings, multiple genes are involved in the inheritance of (a) sickle-cell anaemia (b) skin colour (c) colour blindness (d) phenylketonuria.

Last Answer : ) skin colour

Multiple alleles control inheritance of (a) phenylketonuria (b) colour blindness (c) sickle cell anaemia (d) blood groups.

Description : Multiple alleles control inheritance of (a) phenylketonuria (b) colour blindness (c) sickle cell anaemia (d) blood groups.

Last Answer : (d) blood groups.

Which of the following conditions is not associated with periodontal destruction in primary teeth: a. Down’s syndrome. b. Steven Johnson’s syndrome. c. Hypophosphatasia. d. Papillon. Lefebvre syndrome. e. Cyclic neutropenia.

Description : Which of the following conditions is not associated with periodontal destruction in primary teeth: a. Down’s syndrome. b. Steven Johnson’s syndrome. c. Hypophosphatasia. d. Papillon. Lefebvre syndrome. e. Cyclic neutropenia.

Last Answer : b. Steven Johnson’s syndrome.

Which of the following conditions is not associated with periodontal destruction in primary teeth: A. Down’s syndrome B. Steven Johnson’s syndrome C. Hypophosphatasia D. Papillon-Lefebvre syndrome E. Cyclic neutropenia

Description : Which of the following conditions is not associated with periodontal destruction in primary teeth: A. Down’s syndrome B. Steven Johnson’s syndrome C. Hypophosphatasia D. Papillon-Lefebvre syndrome E. Cyclic neutropenia

Last Answer : B. Steven Johnson’s syndrome

Down’s syndrome is caused by an extra copy of chromosome number 21. What percentage of offspring produced by an affected mother and a normal father would be affected by this disorder? (a) 100% (b) 75% (c) 50% (d) 25%

Description : Down’s syndrome is caused by an extra copy of chromosome number 21. What percentage of offspring produced by an affected mother and a normal father would be affected by this disorder? (a) 100% (b) 75% (c) 50% (d) 25%

Last Answer : (c) 50%

People with Down's syndrome invariably affected by: (1) Huntington's disease (2) Alzheimer's disease (3) Meningitis (4) Brain haemorrhage

Description : People with Down's syndrome invariably affected by: (1) Huntington's disease (2) Alzheimer's disease (3) Meningitis (4) Brain haemorrhage

Last Answer : (2) Alzheimer's disease Explanation: The best-known and most common chromosome abnormality in humans is Down's syndrome, a condition associated with an extra chromosome 21. Down's syndrome individuals ... develop this disease in their fourth or fifth decade of life, much sooner than other people

.********* disease is another name for (a) haemophilia B (b) hepatitis B (c) Down’s syndrome (d) sleeping sickness.

Description : .Christmas disease is another name for (a) haemophilia B (b) hepatitis B (c) Down’s syndrome (d) sleeping sickness.

Last Answer : a) haemophilia B

Which of the following is NOT characteristic of Down’s syndrome? A. Decreased neutrophil function B. Macroglossia C. Macrodontia D. An increased susceptibility to periodontal disease E. Congenitally missing teeth

Description : Which of the following is NOT characteristic of Down’s syndrome? A. Decreased neutrophil function B. Macroglossia C. Macrodontia D. An increased susceptibility to periodontal disease E. Congenitally missing teeth

Last Answer : C. Macrodontia

Which of the following is NOT characteristic of Down’s syndrome? A. Decreased neutrophil function B. Macroglossia C. Macrodontia D. An increased susceptibility to periodontal disease E. Congenitally missing teeth

Description : Which of the following is NOT characteristic of Down’s syndrome? A. Decreased neutrophil function B. Macroglossia C. Macrodontia D. An increased susceptibility to periodontal disease E. Congenitally missing teeth

Last Answer : C. Macrodontia

Typical features of Down’s syndrome (Mongolism) do not include: A. Multiple immunodeficiencies B. Sever caries but minimal periodontal disease C. Susceptibility to infections D. Multiple missing teeth and malocclusion E. Hepatitis B carriage in institutionalised patients

Description : Typical features of Down’s syndrome (Mongolism) do not include: A. Multiple immunodeficiencies B. Sever caries but minimal periodontal disease C. Susceptibility to infections D. Multiple missing teeth and malocclusion E. Hepatitis B carriage in institutionalised patients

Last Answer : B. Sever caries but minimal periodontal disease

People with Down’s syndrome invariably affected by: (1) Huntington’s disease (2) Alzheimer’s disease (3) Meningitis (4) Brain haemorrhage

Description : People with Down’s syndrome invariably affected by: (1) Huntington’s disease (2) Alzheimer’s disease (3) Meningitis (4) Brain haemorrhage

Last Answer : Alzheimer’s disease 

Sickle-cell anemia is a disease caused due to the abnormality in – (1) white blood cells (2) red blood cells (3) thrombocytes (4) blood plasma composition

Description : Sickle-cell anemia is a disease caused due to the abnormality in – (1) white blood cells (2) red blood cells (3) thrombocytes (4) blood plasma composition

Last Answer : (2) red blood cells Explanation: Sickle cell anemia (sickle cell disease) is a disorder of the blood caused by an inherited abnormal hemoglobin (the oxygencarrying protein within the red blood cells).

Abnormal chain of amino acids in sickle cells anaemia is (A) Alpha chain (B) Beta chain (C) Gama chain (D) Delta chain

Description : Abnormal chain of amino acids in sickle cells anaemia is (A) Alpha chain (B) Beta chain (C) Gama chain (D) Delta chain

Last Answer : Answer : B

Klinefelter's syndrome phenotype. -Biology

Description : Klinefelter's syndrome phenotype. -Biology

Last Answer : answer:

.In Drosophila, the XXY condition leads to femaleness whereas in human beings the same condition leads to Klinefelter’s syndrome in male. It proves (a) in human beings Y chromosome is active in sex determination (b) Y chromosome is active in sex determination in both human beings and Drosophila (c) in Drosophila Y chromosome decides femaleness (d) Y chromosome of man have genes for syndrome.

Description : .In Drosophila, the XXY condition leads to femaleness whereas in human beings the same condition leads to Klinefelter's syndrome in male. It proves (a) in human beings Y chromosome is active in ... (c) in Drosophila Y chromosome decides femaleness (d) Y chromosome of man have genes for syndrome.

Last Answer : (a) in human beings Y chromosome is active in sex determination

5. Klinefelters syndrome has the genetic make up (a) 44 autosomes + xxy(b) 44 autosomes + xo (c) 45 autosomes + xx (d) 45 autosomes + xy

Description : 5. Klinefelters syndrome has the genetic make up (a) 44 autosomes + xxy(b) 44 autosomes + xo (c) 45 autosomes + xx (d) 45 autosomes + xy

Last Answer : (a) 44 autosomes + xxy

Which one of the following conditions correctly describes the manner of determining the sex? (a) Homozygous sex chromosomes (ZZ) determine female sex in birds. (b) XO type of sex chromosomes determine male sex in grasshopper. (c) XO condition in humans as found in Turner’s syndrome, determines female sex. (d) Homozygous sex chromosomes (XX) produce male in Drosophila.

Description : Which one of the following conditions correctly describes the manner of determining the sex? (a) Homozygous sex chromosomes (ZZ) determine female sex in birds. (b) XO type of sex chromosomes ... s syndrome, determines female sex. (d) Homozygous sex chromosomes (XX) produce male in Drosophila.

Last Answer : (b) XO type of sex chromosomes determine male sex in grasshopper.