Considering the genetics of Lesch–Nyhan syndrome, explain how a female could inherit the disease considering that afflicted male patients do not have offspring.

Q: Describe the phenotype of individuals who inherit two copies of the HbS allele-Sickle Cell Disease.

A: Sickle cell anemia  It is a genetic disorder that affects erythrocytes(RBC) causing them to become…

Q: What are the reasons why most of the clinical features of the diseases in krebs cycle involve muscle…

A: The Krebs cycle occurs in the mitochondria. It occurs in every cell where oxygen is used to produce…

Q: Explain why a woman carrying the gene forhemophilia can produce two hemophiliac sonswhen she is…

A: A disorder in which blood doesn't clot normally because of a lack of sufficient blood-clotting…

Q: This autosomal dominant disease typically presents in early childhood with a wide clinical spectrum…

A: Many human disorders are hereditary in nature. A genetic disease is a condition that is caused…

Q: Write the name of lysosomal storage disorders.

A: Lysosomal storage disorder are also known as sphingolipidoses, in which sphingolipids are…

Q: Explain why it is not possible for two parents, one with type AB blood and the other with type O…

A: Blood group is classified based on the presence and absence of antibodies and inherited antigenic…

Q: proposed marriage to a nonpolydactylous, astigmatic, blue-eyed, and curly-haired lady whose mother…

A: Astigmatism is an eye illness in which the cornea or lens curvature is altered, resulting in blurred…

Q: Show the cross between a ggBb and a GGBB.

A: gB gb gB gb GB GgBB GgBb GgBB GgBb Gb GgBb Ggbb GgBb Ggbb GB GgBB GgBb GgBB GgBb Gb GgBb…

Q: A man with thalassemia minor marries a normal woman.  What phenotypic ratios of thalassemia-affected…

A: Thalassemia is an inherited blood disorder in which the body makes an abnormal form of hemoglobin.…

Q: Which of the following is FALSE regarding sickle cell anemia? O it is an advantage to be a…

A: Blood is a fluid connective tissue comprised of red blood cells (RBC), white blood cells (WBC),…

Q: Sickle cell anemia is an inheritable red blood cell disorder that results in sickle-shaped red blood…

A: HbA encodes normal phenotype. This allele is dominant over HbS allele.

Q: Explain the cause of Klinefelter​s syndrome. Give any four symptoms shown by sufferer of this…

A: Normally human have 22 pairs of autosomes and 1 pair of sexual chromosomes. Trisomy is a condition…

Q: True or False: An individual with sickle-cell anemia is caused by a missense mutation.

A: Missense mutation is a type of genetic alteration in which a single base pair substitution alter…

Q: Match the Disorder to its description for numbers 11-15:

A: Any disorder of the nervous system leads to a neurological disorder. Any structural, electrical or…

Q: Determine the reason due to which it is possible that the translation of a single mitochondrial…

A: Given that tRNAs are impacted by numerous clinical mitochondrial illnesses brought on by mutations…

Q: What is Down's syndrome? Give its symptoms and cause. Why is it that the chances of having a child…

A: Human genetic disorders are caused by the absence, excess, or abnormal arrangement of one or more…

Q: I read that vinyl chloride exposure is associated with an increased risk of a rare form of liver…

A: Cancer is the condition of uncontrolled cell division.

Q: is lysosomal storage disease linked to ethnicity of human

A: "Lysosomal storage diseases" (LSDs) are hereditary disorders in which the functioning of a lysosome…

Q: Define the following terms: a. coated pit b. familial hypercholesterolemia c. xanthoma d. homozygote…

A: The following terms are explained below, which is as follows:

Q: Jacob and Patau Syndromes List the similarities and differences between these two syndromes. Which…

A: Jacob syndrome: Also known as XYY syndome/ XYY karyotype/ YY syndrome Patau syndrome:  Also known as…

Q: A woman diagnosed with Alzheimer disease wants to know the probability that her children will…

A: Alzheimer's disease or senile dementia is a chronic neurodegenerative disease in which the patient’s…

Q: Describe what are missense mutations and its effects on structure and function using haemoglobin as…

A: A missense mutation may be a mistake within the DNA which ends up within the wrong aminoalkanoic…

Q: Mention any two autosomal genetic disorders with their symptoms.

A: Introduction The two autosomal genetic disorders with their symptoms are as follows.

Q: Why doesn't sickle cell anemia "prove" the existence of biological race?

A: *sickle cell Anaemia is a inherited blood disorder  *This disease produce abnormal haemoglobin  in…

Q: The human male never passes on the gene for haemophilia to his son. Why is it so?

A: Haemophilia is an inherited genetic disorder, which impairs the ability of the body to stop bleeding…

Q: Which of the following disorders arises from translocation events?   Huntington’s disease   Burkitt…

A: Translocation is caused due to separation of a chromosome segment and its union toa nonhomologous…

Q: The DNA located inside of mitochondria exhibits approximately ten times the mutation rate seen in…

A: Mitochondria is a double membrane-bound cell organelle that is used to generate ATP molecules…

Q: Give the name for this molecule: II CH3CH2CH,CH,-ċ-O-H

A: Penotanoic acid, also called as Valeric acid. It is a straight-chain alkyl carboxylic acid. Volatile…

Q: Colour blindness is a sex linked disorder caused by a recessive allele carried on the X chromosome.…

A: color blindness is inherited as a recessive trait on the X chromosome. This is known in genetics as…

Q: Mention Mendelian laws and how they fit in with sickle cell anaemia Are there any advantages to…

A: Introduction :- Sickle cell anaemia is an inherited red blood cell condition in which the body's…

Q: A normal woman marries a man with sickle-cell trait. What is the probability of their having a (a)…

A:

Q: Name the misfolded protein associated with each of the following diseases: Alzheimer’s,…

A: The sequence of amino acids makes the primary structure of the protein. The primary structure folds…

Q: Question 21:  Write the characteristics clinical features of Von Gierke's disease.

A: Von Gierke's disease is a glycogen storage disorder whic occur due to deficiency of enzyme…

Q: Describe two mutations that are associated with the development of leukaemia and how these two…

A: The type of cancer that will begin in the blood-forming tissue, generally in the bone marrow, is…

Q: а. Differences between: i. Wakana's disease from Loeffler's syndrome

A: Note: As Per Guidelines, We Can Answer One Question At A Time. Ask Again To get rest answers.…

Q: Which of the following best explains how individuals who inherit phenylketonuria alleles can avoid…

A: Phenylketonuria is an inherited disorder that increases the level of phenylalanine in the blood of…

Q: name/identify the following:

A: Monocots and Dicots are major angiosperm groups in the plant kingdom. Monocot plants are those which…

Q: This asymptomatic disorder, typically discovered accidentally, is caused by mutations in the SLC36A2…

A: Both the mutations are associated with Iminoglycinuria

Q: Explain the consequence of the following structures.

A: The given structure represents the phospholipid molecules in a lipid bilayer. Phospholipids are…

Q: Why do sons of haemophilic father never suffer from this trait?

A: Haemophilia is an inherited genetic disorder, which impairs the ability of the body to stop bleeding…

Q: what fraction of the offspring of two parents with sickle trait would you expect to have sickle cell…

A: Sickle cell anemia is one of a group of blood disorders known as sickle cell disease. It affects the…

Q: Sickle-cell anemia is a genetic disorder of individuals homozygous for a mutation of hemoglobin that…

A: Sickle cell anemia is an autosomal disease in which the red blood cells become sickle-shaped. In…

Q: Difference between klinefilter syndrome and turner's syndrome?

A: Any gain or loss in the number of chromosomes number, or any change in the structure of the…

Q: Given the information regarding sickle cell anemia, if two carriers were to have children, what…

A: Sickle-cell disease is a condition of the blood wherein the structure of the hemoglobin within the…

Q: What is Patient B's karyotype? A. Klinefelter syndrome B. Trisomy 13 syndrome C. Down syndrome…

A: Introduction : Karyotype : Karyotype is a representation of  complete set of metaphasic chromosome…

Q: Define these pairs of terms, and distinguish between them. Patau syndrome/Edwards syndrome

A: Some chromosomal disorders are caused due to change in the number of chromosomes in the offspring.…

Q: According to information from the following three cases, what conclusion can you make regarding the…

A: The clinical manifestation of a disease is subjective when it is perceived by the patient or may be…