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If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is ______. - Biology

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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

MCQ
रिक्त स्थान भरें
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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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  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 5: Principle of Inheritance and Variation - MULTIPLE CHOICE QUESTIONS [पृष्ठ २९]

APPEARS IN

एनसीईआरटी एक्झांप्लर Biology [English] Class 12
अध्याय 5 Principle of Inheritance and Variation
MULTIPLE CHOICE QUESTIONS | Q 4. | पृष्ठ २९
नूतन Biology [English] Class 12 ISC
अध्याय 5 Principles of Inheritance and Variation
Test Your Progress | Q 1. 94. | पृष्ठ २००

संबंधित प्रश्न

About 8% of the human male population suffers from colour blindness, whereas only about 0.4% of the human female population suffers from this disease. Write an explanation to show how it is possible.


What do sex linked traits appear in males than in females? 


Very Short Answer Question.

Give an example of a chromosomal disorder caused due to nondisjunction of autosomes.


What is the reason for the 21st trisomy?


What are the different characters that develop due to Klinefelter's syndrome?


Match the Column-I with Column-II and choose the CORRECT answer

  Column-I   Column-II
P.  Klinefelter syndrome i. Mutation in autosomal gene
Q. Thalassaemia ii. Mutation sex chromosome linked gene
R. Down syndrome iii. Trisomy of autosome
S. Colour blindness iv. Trisomy of sex chromosome

Mental retardation in man associated with sex chromosomal abnormality is usually due to ______.


Trisomy is represented by ______.


Read the following and answer from given below:

Turner's syndrome is an example of monosomy. It is formed by the union of an allosome-free egg and a normal 'X' containing sperm or a normal egg and an allosome-free sperm. The individual has 2n = 45 chromosomes (44 + X0) instead of 46. Such individuals are sterile females who have rudimentary ovaries, underdeveloped breasts, small uterus, short stature, webbed neck, and abnormal intelligence. They may not menstruate or ovulate. This disorder can be treated by giving female sex hormones to women from the age of puberty to make them develop breasts and have menstruation. This makes them feel more normal.

Which of the following statements regarding Turner's syndrome is incorrect?


What are chromosomal disorders?


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