While studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this sign was founded only in the men and it was inherited from father to the son. Define the type of hypertrichosis inheritance? Select one: a. Y-linked b. Autosomal-recessive c. Autosomal-dominant d. Recessive, X-linked e. Dominant, X-linked
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- Which of the following does not have an autosomal recessivepattern of inheritance?a. cystic fibrosisb. Huntington diseasec. phenylketonuriad. sickle cell diseasee. None of these are correct.a. The ability to taste the chemical phenylthiocarbamideis an autosomal dominant phenotype, and the inabilityto taste it is recessive. If a taster woman with a nontasterfather marries a taster man who in a previous marriagehad a nontaster daughter, what is the probability thattheir first child will be(1) A nontaster girl(2) A taster girl(3) A taster boyb. What is the probability that their first two childrenwill be tasters of either sex?Review the process of autosomal dominant inheritance by coloring the following figures. In this instance the father is affected in the mother is unaffected to illustrate the transmission of the disorder from the father to the children color the figures as described.
- Albinism is a recessive autosomal trait for skin pigmentation. Hemophilia is a sex-linked recessivedisorder of the blood. assign alleles to the traitsA – normal skin pigmentation X H – normal blooda – albino X h - hemophilia A double heterozygous woman marries a non-hemophilic man and heterozygous for skinpigmentation. Double heterozygous means heterozygous for both traits. Aa for skin pigmentation andX H X h for blood trait. Therefore, the genotype of the woman is AaX H X h . Non-hemophilic man is X H Y and heterozygous for skin pigmentation is Aa. The genotype,therefore, of the man is AaX H Y. What is the probability that they will have:a. a child with normal skin? _____________________b. a child with normal blood? _____________________c. an albino girl? _____________________d. A hemophilic boy? _____________________1) Symptoms of 4 disorders are listed. Using the lists given, fill in the correct letter for the condition name and inheritance type. Letters may be used more than once. Symptoms Condition Inheritance Туре Loss of muscle control and decline in mental ability Shades of red and green are hard to distinguish Lack of skin pigmentation Cannot produce one of the necessary blood clotting factors Conditions: Inheritance Type: A: Albinism E: X-linked dominant B: Huntington Disease F: X-linked recessive G: Y-linked C: Hemophilia H: Autosomal dominant I: Autosomal recessive D: CVDAaBbCcDc AaBbCcD Ac Heading 1 Heading 2 Title Subtitle Subtle Em.. Emphasis Intense E... Strong Quote Int Paragraph Styles 4 Genetic Inheritance Patterns Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. gene from your Mom and one from your Dad). Autosomal means it is not Question below short answer approach image you are the genetics counselor, should Eric have children? Imagine he has a daughter (he has two, but both are adopted). What advice would you give Eric if his wife was a carrier from a genetics counseling viewpoint? Describe all the possibilities,…
- Match the mode of inheritance with its description. (1) autosomal recessive A. inherited by males from carrier mothers(2) autosomal dominant B. inherited from one affected parent(3) X-linked recessive C. inherited from two carrier (unaffected) parentsCystic fibrosis (CF) is an autosomal recessive condition triggered by the overproduction of stickymucus that clogs the lungs and pancreas. It is a life-threatening disease, but medical advances helpedthe afflicted to live through adulthood.The mother of Claudia died from cystic fibrosis, but her father was normal and never had anyrelative with CF. Her fiancé, Marcus, turned out to be a carrier of the CF allele. What are the genotypes of Claudia and Marcus? Claudia: ________________________ Marcus: _____________________ They planned to have four children. What is the probability that: a. all children will be normal b. at least two will be normalCystic fibrosis (CF) is an autosomal recessive condition triggered by the overproduction of stickymucus that clogs the lungs and pancreas. It is a life-threatening disease, but medical advances helpedthe afflicted to live through adulthood. The mother of Claudia died from cystic fibrosis, but her father was normal and never had anyrelative with CF. Her fiancé, Marcus, turned out to be a carrier of the CF allele. What are the genotypes of Claudia and Marcus? Claudia: ________________________ Marcus: _____________________ They planned to have four children. What is the probability that:a. all children will be normal b. at least two will be normal
- Explain the sex-linked traits. (S9LT-ld-29.4.4) Solve problems related to sex-linked traits. (S9LT-ld-29.4.4) WHAT I NEED (MATERIALS) • Worksheet • Pens WHAT TO DO (PROCEDURE) PART A Directions: Tell whether the following carry or show the sex-linke recessive spongy-tiny pores trait. Also, tell whether the individuals a male or female. Remember that since most sex-linked traits are recessive, the person w shows the trait can have no X's with big superscripted letters. So, if a m carries the trait, he must also show the trait. XDY XDXD XdY Carrier? (Yes or No) Has the Trait? (Yes or No) Male or Female Phenotype or Appearance of the Individual ided Questions: 1. What chromosomes will result to a normal phenotype (normal spongy po trait12Review the process of autosomal recessive inheritance by coloring the following figures in this instance both parents are carriers of a treat to illustrate the transmission of the disorder from the parents to the children color the figures as describedWhich of the following can be identified by anabnormal karyotype?a. Sickle cell diseaseb. Cystic fibrosisc. Monosomy Xd. Tay-Sachs diseasee. Huntington’s chorea