मराठी
महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

Mention the symptoms of Down syndrome. - Biology

Advertisements
Advertisements

प्रश्न

Mention the symptoms of Down syndrome.

Mention any six symptoms of disorder caused by trisomy of 21 chromosome.

लघु उत्तर
Advertisements

उत्तर

  1. Mental retardation, either mild or moderate.
  2. Skeletal underdevelopment.
  3. Unique facial characteristics, such as a small mouth, ears, and head.
  4. Usually round and flat, with an open mouth and a flat nose.
  5. Protruding tongue.
  6. The inner corner of the eyes is covered by an epicanthal skin fold.
  7. Slanting eyes.
  8. Broad palms with a single Palmer crease; flat hands with stubby fingers.
shaalaa.com

Notes

Students should refer to the question according to their questions and preferred marks.

  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 4: Principles of Inheritance and Variation - Evaluation [पृष्ठ ५६]

APPEARS IN

सामाचीर कलवी Biology (Zoology) [English] Class 12 TN Board
पाठ 4 Principles of Inheritance and Variation
Evaluation | Q 29. | पृष्ठ ५६
सामाचीर कलवी Biology (Zoology) [English] Class 12 TN Board
पाठ 4 Principles of Inheritance and Variation
Evaluation | Q 32. | पृष्ठ ५९

संबंधित प्रश्‍न

Klinefelters’ syndrome is characterized by a karyotype of ____________.


Females with Turners’ syndrome have


Pataus’ syndrome is also referred to as ____________.


Which of the following is not correct?


What is Down’s syndrome? Give its symptoms and cause. Why is it that the chances of having a child with Down’s syndrome increases if the age of the mother exceeds forty years?


How was it concluded that genes are located on chromosomes?


Define aneuploidy. How is it different from polyploidy? Describe the individuals having following chromosomal abnormalities.

  1. Trisomy of 21st Chromosome
  2. XXY
  3. XO

The chromosome number is fixed for all normal organisms leading to species specification whereas any abnormality in the chromosome number of an organism results into abnormal individuals. For example, in humans, 46 is the fixed number of chromosomes both male and female. In males it is '44 + XY' and in females, it is '44 +XX'. Thus the human male is heterogametic, in other words produces two different types of gametes one with '22 + X' chromosomes and the other with '22 + Y' chromosomes respectively. Human female, on the other hand, is homo gametic i.e. produce only one type of gamete with '22 + X' chromosomes only.

Sometimes an error may occur during the meiosis of the cell cycle, where the sister chromatids fail to segregate called nondisjunction, leading to the production of abnormal gametes with altered chromosome numbers. On fertilisation, such gametes develop into abnormal individuals.

(a) State what is aneuploidy. (1)

(b) If during spermatogenesis, the chromatids of sex chromosomes fail to segregate during meiosis, write only the different types of gametes with altered chromosome numbers that could possibly be produced. (1)

(c) A normal human sperm (22 + Y) fertilises an ovum with karyotype '22 +XX'. Name the disorder the offspring thus produced would suffer from and write any two symptoms of the disorder. (2)

OR

(c) Name the best-known and most common autosomal aneuploid abnormality in humans and write any two symptoms. (2)


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×