English

Give the Genotype of Turner’S Syndrome.

Advertisements
Advertisements

Question

Give the genotype of Turner’s syndrome.

One Line Answer
Advertisements

Solution

The genotype of Turner’s syndrome is represented by (44 + XO).

shaalaa.com
  Is there an error in this question or solution?
2015-2016 (March)

APPEARS IN

Video TutorialsVIEW ALL [2]

RELATED QUESTIONS

Why are thalassemia and haemophilia categorized as Mendelian disorders? Write the symptoms of these diseases. Explain their pattern of inheritance in humans.


During a medical investigation, an infant was found to possess an extra chromosome 21. Describe the symptoms the child is likely to develop later in the life.


State any two symptoms of Down’s syndrome.


Webbed neck is characteristic of ______ syndrome.


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


Identify the characteristics that are observed in an individual suffering from Klinefelter syndrome.

i. Gynaecomastia, under developed testis and no spermatogenesis.

ii. Voice pitch is harsh.

iii. They are tall with long arms.


Sickle cell anaemia is ______.


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.

The number of Barr bodies present in a female with Turner's syndrome is ______


If a father and son are both defective in red-green colour vision, is it likely that the son inherited the trait from his father? Comment.


Lipoprotein lipase deficiency (LPLD)is a genetic disorder in which a person has a defective gene for lipase. This leads to high triglycerides, stomach pain, and fat deposits under the skin. It may eventually affect the liver, pancreas and may also cause diabetes. The disorder occurs if a child acquires defective genes from both parents (autosomal recessive). ERT (enzyme replacement treatment) is one of the treatments offered to patients with LPLD.

    1. What procedure is followed in ERT?
    2. What could be one possible drawback of ERT?
  1. How can LPLD be treated using Biotechnology? Elaborate.

Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×