Mutations of the CFTR gene causes ( Cerebral Plasy or Cystic Fibrosis or Craniofacial timbrosis or Fragile X syndrome). ? Which is (a/an) (Autosomal Dominant or X-linked ressessive or X-linked dominat or Recessive Deleterious)

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: Amelogenesis imperfecta A faulty tooth enamel formation. Dominant traits Autosomal dominant allele…

Q: Suppose that a female with the mutation (i.e., a heterozygous female) mates with a healthy male (the…

A: Alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: cance of color blindness in humans is due to a recessive gene located on the X chromosome X linked).…

A: Mother     ×      father            XXc                  XcY Progeny -      X Xc Xc XXc…

Q: Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently…

A: Autosomal recessive disease occurs when a child acquires both the mutated allele from both the…

Q: A woman develops Huntington's disease and already has 3 children. What is the chance that the mother…

A: Huntington’s disease or Huntington's chorea is a muscular and mental disorder. There is a gradual…

Q: Cystic fibrosis is an autosomal recessive disorder that affects 1 in 3 000 newborns with Caucasian…

A: Cystic fibrosis is a life-threatening heredity disorder that affects the lungs and the digestive…

Q: Question 94 (Mandatory) Duchenne muscular dystrophy is inherited in an X- linked recessive pattern.…

A: Duchenne Muscular Dystrophy (DMD) is an X-linked recessive condition, which implies the changed gene…

Q: The mutations found in the HD allele result in a protein that has normal activity. The pattern of…

A: In this answer, we will explore genetic inheritance patterns and the specific case of Huntington's…

Q: Achondroplasia, which is characterized by difficulty converting cartilage to bone and thus results…

A: Hhsbanf is colorblind i.e XcY  Wife is carrier as their son and daughter both are affected .i.e XCX…

Q: which genetic disorder matches below descriptions. extra 21st chromosome attaches to chromosome 14.…

A: Genetic disorder is defined as the disease caused by the abnormality in the genome of an organism.…

Q: Hemophilia is another example of a X-linked disease caused when a recessive allele (Xh) is…

A: Hemophilia is a disorder where blood clots do not form normally which leads to excessive bleeding…

Q: questions: Red-green colorblindness is a recessive X-linked genetic disorder. A normal-vision male…

A: Colour blindness is a genetic disorder in which an individual is unable to perceive the true colours…

Q: For the following diseases with their potential pedigree, mode of inheritance and the responsible…

A: Pedigree B, Autosomal dominant, FGFR3 geneAchondroplasiaPedigree B, Autosomal dominant, Huntingtin…

Q: Geneticists are concerned about three different genetic conditions present within their family.…

A: Autosomal dominant A = achondroplasia  a = average height  AA and Aa = affected aa = normal    X…

Q: A man and woman are both affected by an autosomal dominant disorder, polydactly. Their first child…

A: The alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: Inherited cancers are due to mutations in ________ cells. They are/are not passed on to offspring.…

A: Cancer is a disease where some cells of the body divide uncontrollably and they can also infiltrate…

Q: Please explain Androgen Insensitivity Syndrome (ALS). What is the phenotype of these individuals?…

A: The common etiology of aberrant sexual development, androgen insensitivity syndrome, results in a…

Q: Which genotype indicates a carrier of an autosomal recessive trait?   bb   BB   Bb

A: The dominant allele (represented by capital letter  'B' )  can show its character in the phenotype…

Q: (a) What pattern of transmission is most consistent with this pedigree? (1) autosomal recessive, (2)…

A: Pedigree  A family tree or chart that represents a person's genetic family history by symbols and…

Q: In autosomal dominant disorders, the recurrence risk is ¾(75%) when one affected parent and one…

A: When a child receives one version of a mutant gene from one parent, autosomal dominant inheritance…

Q: Autosomal Dominant Disorder: Huntington's Disease 1. Huntington's disease is a neurological disease…

A: The alleles are alternative forms of a gene that are located on the same locus of a homologous…

Q: A woman develops Huntington's disease and already has 3 children. What is the chance that the mother…

A: Huntington’s disease or Huntington's chorea is a muscular and mental disorder. There is a gradual…

Q: Achondroplasia, which is characterized by difficulty converting cartilage to bone and thus results…

A: The alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: Q7. Haemophiliacs possess a non-functional form of the gene responsible for the production of blood…

A: Answer :- Dominant allele = H Recessive allele = h Supercript on X are xH and xh xH =Dominant  xh=…

Q: Please answer with reason: 1) The nurse is explaining the inheritance of Huntington disease…

A: Autosomal dominant is a pattern of inheritance in which an individual has one mutant allele and one…

Q: Neurofibromatosis-1 (NF1) is an autosomal dominant disorder where tumours form in the base layer of…

A: The probability is 1/4

Q: Berries → titmouse → snake → buzzard 6,000 calories

A: A food chain is a sequence of organisms that feed on the previous organism. Several food chains…

Q: Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an…

A: Genes are the unit of inheritance that transfers traits from one generation to another. Genes coding…

Q: B A In the image above, the tissue found at letter B is; Нaploid Diploid Neither

A: The above image belongs to the ferns. It is the prothallus of the fern developed from spores.

Q: Autosomal aneuploidy is usually lethal due to genetic_________

A: Introduction  Chromosomal aberrations are the common cause of abnormal development of the embryo or…

Q: Match the following with their appropriate descriptor: 1. Homozygous Dominant hh xhy 2. Heterozygous…

A: Homozygous Individuals carrying two identical alleles (RR or rr) are known as homozygous.…

Q: For the following diseases with their potential pedigree, mode of inheritance and the responsible…

A: Detailed explanation: Let's analyze Pedigree C, which is an X-linked recessive pedigree related to…

Q: Classify the following conditions based on whether they are describing autosomal dominance,…

A: Genetics is a study of genes, heredity, and genetic variation in an organism. Living organisms…

Stress

Stress is defined as the feeling of being overwhelmed or unable to cope with emotional or mental pressure. Any event or action that makes a person annoyed, furious, or nervous can trigger it. Chemical changes in the body caused by stress can cause blood pressure, blood sugar levels, and heart rate to rise.