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प्रश्न
Identify ‘a’, ‘b’, ‘c’, ‘d’, ‘e’ and ‘f’ in the table given below:
| S. No. | Syndrome | Cause | Characteristics of affected individuals | Sex (male/female/both) |
| 1. | Down’s | Trisomy of 21 |
‘a’ |
‘b’ |
| 2. | ‘c’ | XXY | Overall masculine development | ‘d’ |
| 3. | Turner’s | 45 with XO |
‘e’ |
‘f’ |
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उत्तर
| No | Syndrome | Cause | Characteristics of affected individuals |
Sex/Male/Femal e/Both |
| 1. | Down’s | Trisomy of 21 |
(i) Broad forehead (ii) Permanently open mouth, protruding and furrowed tongue and projecting lower lip. |
Both |
| 2. | Klinefelter’s | XXY | Overall masculine development | Male |
| 3. | Turner’s | 45 with XO |
(i) Poorly developed ovaries, webbed neck, broad chest with under developed breasts and below average intelligence. (ii) Body hair absent |
Female |
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संबंधित प्रश्न
If only one 'X' chromosome is found in a female person, which of the following symptoms she will show?
- epicanthal skin fold
- webbing of neck
- small testis and absence of spermatogenesis
- presence of simian crease on the palm
A colour-blind child is born to a normal couple. Work out a cross to show how it is possible. Mention the sex of this child.
Give an example of a human disorder that is caused due to a single gene mutation.
Match Column I with Column II and select the correct option:
| Column I | Column II | ||
| p. | Pleiotropy | I. | More than two alleles occur at the same locus on homologous chromosomes |
| q. | Multiple alleles | II. | Expression of both the alleles m heterozygous condition |
| r. | Polygenic | III. | Multiple effect of single gene |
| s. | Co-dominance | IV. | Single phenotypic character influenced by more than two genes |
Choose the correct option which appropriately classifies the following disorders into Mendelian and chromosomal disorders:
Colour blindness, Down syndrome, Sickle cell anaemia, Turner syndrome, Thalassemia, Haemophilia, Phenylketonuria, Klinefelter syndrome.
Where are the genes for cytoplasmic male sterility in plants located?
This abnormality occurs due to monosomy (2n - 1); the individual has 2n = 45 chromosomes with 44 + XO genotype.
In Down's syndrome, karyotyping has shown that the disorder is associated with trisomy of chromosome number 21 usually due to ______.
Select the correct match.
Describe Turner's syndrome.
