reate a profile of a human chromosomal disorder. the chromosome disorder can be autosomal or sex linked. be sure to have definition, autosomal/sex linked, treatment options, symptoms, and one other bit of information you find interesting (mortality, frequency, etc)

Q: disease, its prevalence and options. As a genetic counselor, your next responsibility is to take a…

A: Cystic fibrosis is a severe life threatening disease that affects the lungs, digestive system and…

Q: s alternative form of a single gene is known as  parental, dihybrid, reciprocal, allele, or…

A: Alleles are variant forms of a gene. Individuals receive one allele from the father and one from the…

Q: What are genetic disorder that cause by the following substances/product? Just give one genetic…

A: Genetic disorders are diseases caused in whole or in part by a change in the DNA sequence away from…

Q: discusses the role of genetics in health status. Do you believe that genetic testing can be helpful…

A: Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or…

Q: 3 List some common sex-linked human diseases. Type answer here. Your a 4 List some common autosomal…

A: Autosomes are the chromosomes that carry genes for all the functions except the sex determination.

Q: Which of the following genetic disorders is described by the following: Recessive sex-linked…

A: Only the X chromosome contains the 'gene' that induces (inherited, red and green forms of) colour…

Q: QUESTION 10 Hypertrichosis is an unusual disease, but it is not a fatal disorder in either the…

A: Autosomal dominant is a pattern of inheritance where a single copy of a mutated gene from one parent…

Q: The inherited component of a phenotype is determined by the:     age of the organism…

A: Phenotype simply means a distinguishable characteristic.  Pheno, which has the same root as the…

Q: When an individual has genome mutations, their chromosome structure changes. True or False.

A: Mutations are sudden heritable change in the genetic make up of an individual which alters the amino…

Q: Assume that you are a genetic counsellor and analyzing RFLP pattern for a family with three…

A: RFLP is an analytical technique that uses restriction endonucleases to determine whether a…

Q: PKU disease is recessive. A man and a woman are both carriers for PKU disease. Determine the…

A: KU disease is recessive. A man and a woman are both carriers of PKU disease. NormALLELE---------P;…

Q: Common red-green color blindness is an X-linked trait. A woman whose father is color blind married a…

A: Red-green colorblindness is caused due to the mutation on X-chromosome in a recessive manner. So,…

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: animal breeding: heritability // answer the question precisely and detailed.

A: Genetic progress is defined as the progress that is made when the average genetic value of the…

Q: ISB 603 Karyotype #5 designation: (hint: this is not a deletion) Genetic condition:

A: Step 1: Step 2: Step 3: Step 4:

Q: What would the most likely genotype be for a person exhibiting a rare single gene Autosomal…

A: Mutations in genes situated on autosomes, which are non-sex chromosomes, cause autosomal recessive…

Q: Which of the following describes the pattern of sex chromosomes in this athlete? (Look at picture)…

A: Klinefelter syndrome is characterized by the presence of one extra X chromosome in a male. Many…

Q: In humans, Huntington's Disease is an autosomal dominant trait. Huntington's Disease has late onset,…

A: The woman who had a father not affected and a mother with Huntington's disease is heterozygous, as…

Q: In autosomal dominant,  A child who has a parent with the mutated gene has a 50% chance of…

A: Introduction Disorder:- It is an illness that disrupts normal physical or mental functions,…

Q: Duchenne muscular dystrophy is one of the sex-inherited disease. Write a report about the mutation…

A: Duchenne muscular dystrophy (DMD) is a genetic condition that affects the muscles, leading to muscle…

Q: Explain the following diagram. It refers to a pedigree on the disease called phenylketonuria.…

A: The pedigree analysis describes the process of interpretation of information displayed as a family…

Q: SUBJECT-GENETICS TOPIC: Inheritance Related to Sex Identify some form of abnormalities wherein it…

A: Genetic abnormalities - Genetic abnormalities are conditions caused by changes to the genes or…

Q: Two carriers of the sickle cell disease gene reproduce. What are the possible outcomes for their…

A: Sickle cell anemia: Vernon Ingram in 1957 demonstrated that sickle cell anemia is caused due to the…

Q: TURNER SYNDROME 1. Please describe the ethical considerations for genetic testing while pointing out…

A: Turner syndrome is a chromosomal disorder in which a female is born with only one X chromosome. This…

Q: A gene is a unit of heredity that . All of these answers are true consists of a small strand of…

A:

Q: 5 1 point What is the most likely mode of inheritance of the disease depicted in the following…

A: Pedigree is historical record of of ancestry, showing lineage. It is very useful in finding out the…

Q: list 10 ways how you can help promote awareness and respect for genetic disorders

A: Genetic disorders are the inherited medical conditions caused by the DNA abnormalities. Examples:…

Q: If the given statement is true or false, explain. Over 300 genetic defects can be detected now by…

A: A karyotype is defined as an organized profile of a persons chromosome and we know that a chromosome…

Q: 3 o help you understand which genetic condition could explain each athlete's test resu plete the…

A: Congenital adrenal hyperplasia results from the 21-hydroxylase deficiency is caused by the autosomal…

Q: Genetic disorder is a disease that is caused by an abnormality in an individual’s DNA. Range from a…

A: A genetic disorder is a health issue caused by one or more genomic defects. It may be caused by a…

Q: Select the true statements. (can be multiple).     Sperm and egg cells are diploid, meaning that…

A: Haploid cells contain a single set of chromosomes. Diploid cells contain two sets of chromosomes.

Q: QUESTION 1) Scientists have been studying a population of dragonflies of a remote island in an…

A: Note: Since you have asked three questions and all three are not interrelated, the first one has…

Q: underlying a condition for which there is no Genetic testing involves testing individuals for the…

A: GENETIC TESTING : It is a type of tests that identify change in genes that helps us in understanding…

Q: Match the genetic disorder to the descriptions below: Edward Syndrome Jacob Syndrome Patau Syndrome…

A: Genetic disorders are caused by mutations in the genes and such mutations can be single-gene,…

Q: Assume for a moment that a child has a autosomal recessive disorder, but both parents appear normal.…

A: The autosomal recessive is one of the ways to pass down the trait into generations or families. The…

Q: Part II-Autosomal Dominant Traits "Great, so this looks like an accurate representation of your…

A: Given - Myotonic dystrophy is an autosomal dominant genetic disorder. Greg has an uncle, aunt and…

Q: Red-green color blindness means that a person cannot distinguish shades of red and green (usually…

A: Introduction : Colour blindness is an X - linked recessive disease. So if one X chromosome is…

Q: Phenotypes that are related to the sex can be classified as: sex-linked, sex -limited, or…

A: An example for the sex linked trait is the haemophilia. The traits that are carried on the X…

Q: In mitochondrial disorder, mutation in nuclear DNA may follow autosomal dominant, autosomal…

A: Mitochondrial disease, also known as a mitochondrial disorder, is an umbrella term for a range of…

Q: Susan: ½ Dutch and ½ Irish John: Full German Who in your family has been diagnosed with cystic…

A: Cystic fibrosis is an autosomally inherited disease. This means that when both the alleles are…

Q: Part A What is the probability that the first son of a woman whose brother has Lesch-Nyhan syndrome…

A: Lesch Nyhan syndrome is X linked recessive disorder. Normal = XX, XXn, XY Affected = XnXn, XnY

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.