It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin.

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It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin.

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It is autosomal recessive disorder which is caused by transversion mut...

Symptom of sickle cell anemia?

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It is autosomal recessive disorder which is caused by transversion mut...

Sickle cell anaemia

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Dr. Patel is evaluating a 6-year-old child, Mia, who has been experiencing symptoms of chronic anemia, including fatigue, pallor, and delayed growth. Mia’s parents are concerned because these symptoms have persisted despite regular treatments. Mia’s family history reveals that her parents are both carriers of a genetic blood disorder, and several relatives have similar health issues.Dr. Patel decides to perform genetic testing to identify the underlying cause of Mias anemia. The test results indicate that Mia has an autosomal recessive blood disorder caused by a mutation in the globin genes. Specifically, the test shows that Mias condition is related to the reduced production of α globin chains due to the deletion or mutation of genes on chromosome 16.Based on Mia’s case, which of the following statements accurately describes the disorder she is likely to have?

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Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaSickle cell anaemia is a/an ________________ disease.

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Read the following and answer the questions 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, under developed 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 hormone to the women from the age of puberty to make them develop breasts and have menstruation. This makes them feel more normal.Turner’s syndrome is a/an

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Look at the following pedigree chart. On what basis the trait represented by the solid symbols in the pedigree below cannot be explained?(i) A dominant sex linked gene(ii) A recessive sex linked gene(iii) A holandric gene(iv) A sex limited autosomal dominant(v) A sex limited autosomal recessive(vi) A sex influenced autosonal gene dominat in males(vii) A sex influenced autosomal gene recessive in males

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In a population an autosomal recessive disorder is present in 60 individual out of 6000. What is the no. Of homozygous normal offspring in population?

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It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin.

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It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin. for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin. covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for It is autosomal recessive disorder which is caused by transversion mutation in which glutamic acid is replaced by valine at the 6th position of beta-chain of haemoglobin..

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