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प्रश्न
If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is ______.
विकल्प
Sex-linked recessive
Autosomal dominant
Sex-linked dominant
Autosomal recessive
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उत्तर
If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is sex-linked recessive.
Explanation:
If a genetic disease is passed from a phenotypically normal but carrier female to only some of the male offspring, it indicates a sex-linked recessive inheritance. In such cases, females can be carriers without showing symptoms because they have two X chromosomes, and the defective gene is recessive. Males, having only one X chromosome, exhibit the disease if they inherit the affected X from the carrier mother, leading to the disease manifesting only in some of the male progeny. This pattern is typical for diseases like haemophilia and color blindness.
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संबंधित प्रश्न
Give an example of an autosomal recessive trait in humans. Explain its pattern of inheritance with the help of a cross.
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’ |
Name the disorder caused by under secretion of thyroxine in children
Give reasons for the development of Turner’s syndrome and also mention its symptoms.
A male rabbit of genotype 'AABBDDEE' is crossed with a female rabbit of genotype 'aabbddee' to produce F1 hybrid offspring. How many genetically different gametes can be produced by this F1 hybrid?
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.
A short stature with webbing of neck and low posterior hairline indicates ______ syndrome.
Down’s syndrome is due to ______.
Mongolism is a genetic disorder which is caused by the presence of an extra chromosome number ______.
Klinefelters’ syndrome is characterised by a karyotype of ______.
