A biotechnology company offers a direct-to-consumer test called the Carrier Status report that generates various calculations about an individual’s genetic risk for certain diseases. Write one paragraph that addresses the following two issues: Why would this be most useful for disorders following an autosomal recessive pattern of inheritance? Provide evidence from your textbook (e.g., Section 10.7, Inheritance Patterns in Humans). Explain how this information might be useful for people during their reproductive years.

Q: Regarding Mendelian inheritance in diploid individuals, (Read each statement carefully. Select all…

A: Ploidy is a term which describe the number of sets of chromosomes in a cell. The term haploid…

Q: Huntington disease (HD) is a rare dominant  condition in humans that results in a slow but…

A: Introduction :- Huntington's disease is a degenerative brain disease caused by a single faulty gene…

Q: Cystic Fibrosis (CF) is an autosomal recessive condition. Therefore, heterozygous (Cc) carriers do…

A: As a hereditary counselor, we would direct them through the probabilities of their children…

Q: this disorder? (Is it autosomal dominant? Autosomal recessive? X-linked dominant? X-linked…

A: Inheritance inheritance is described as a pattern of transfer of genes from the parental generation…

Q: Duchenne muscular dystrophy is sex linked and usually affects only males. Victims of the disease…

A: Duchenne muscular dystrophy is recessive sex-linked genetic disorder that typically affects the…

Q: The woman in Problem 24 has had two miscarriages. She has come to you, an established genetic…

A: Miscarriage is normally called pregnancy loss. It refers to the natural death of the embryo and the…

Q: Albinism and sickle cell anemia are both autosomal recessive disorders that are expressed only in…

A: Albinism - genotype be A and a.  aa is diseased, Aa is the carrier and AA is not affected.  Sickle…

Q: Hemophilia is a disease inherited as a X-linked recessive trait while pattern baldness is controlled…

A: Haemophilia is a X-linked recessive trait, and baldness is an autosomal recessive trait. The…

Q: The role of the TPMT genotype in response to treatment emphasizes the importance of…

A: TPMT gene synthesizes an enzyme known as thiopurine methyltransferase. This gene has majorly five…

Q: The figure below shows part of a family tree in which an inherited coagulopathy occurs. Analyze the…

A: Pedigree analysis is used to determine the possibility of genetic diseases in individuals or the…

Q: lease consider the following pedigree. Assume that people who marry in to the family do not carry…

A: The pedigree indicates if the DNA is passed down unchanged from generation to generation. It can…

Q: he propensity to develop retinal cancer can run in pedigrees of certain families. You have learned…

A: Tumor suppressor genes are important cancer prevention genes since a partial or total inactivation…

Q: The questions below all refer to the following pedigree. The locus for allele D/d determines how…

A:

Q: Huntington disease (HD) is a genetic disorder that usually first appears in middle age and, over…

A: Huntington disease (HD) is a progressive brain disorder that causes uncontrolled movements,…

Q: Hypophoshatemia is a dominant genetic disorder caused by deficiency of pho[hates in the blood.…

A: The pattern of inheritance in question involves a genetic disorder related to phosphate deficiency…

Q: A genetics counselor, Nashaly Montez, notices an odd pattern in Devin’s pedigree, a propensity for…

A: Tumor suppressor genes function to control cellular proliferation by negatively regulating cell…

Q: Sheree is referred to a genetic counselor because a cystic fibrosis (CF) test done as a routine part…

A: A hereditary condition known as cystic fibrosis (CF) is autosomal recessive. An individual must…

Genomic studies

Genomic studies (genomics) is the study of the whole genome of an organism. Using bioinformatics and high-performance computing, genomic researchers examined massive amounts of deoxyribonucleic acid (DNA)-sequence data to discover variations or mutations that affect drug response, health, or disease. Genomics is a much younger discipline than genetics, having only emerged in the last few decades as a result of technological advancements in DNA sequencing and computational biology.