The etiology of Down Syndrome can be best described as mental deficiency O three copies of chromosome 21 increased risk of heart defects O detected through the use of ultrasound, blood testing, and amniocentesis
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- Having all the necessary information about chromosomal abnormalities, complete the table below to assess your understanding of all the lessons included.Which of the following methods might have a clue whether child suffering from genetic disease a was missing a large chunk of the jean that one defective caused the genetic disorder?State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntingtons disease, and hemophilia A.
- Give three arguments in support for aborting a child with a chromosomal aberration, and three arguments in choosing to let the child live.Please select all of the following that are x- linked disorders. O Cystic Fibrosis red-green color blindness O Hemophilia Duchenne Muscular Dystrophy O Down SyndromeFragile X syndrome What is the prevalence of the trait or disorder? two paragraphs
- Patient A's History Patient A is the nearly-full-term fetus of a forty year old female. Chromosomes were obtained from fetal epithelial cells acquired through amniocentesis. Patient A's Karyotype See attached picture 1. Using the correct notation for interpreting karyotypes, give your diagnosis for the conditions of each patient. (standard notation and phenotype (e.g. 47, XY, +21, male Down syndrome)): References1. Give the genetic cause (chromosomal abnormality and genes affected), and major characteristics of the syndrome Miller Dieker syndrome Wolf-Hirschhorn syndrome Chronic myeloid leukemia/Philadelphia chromosome Acute promyelocytic leukemia Cri-du-chatMatch the chromosome disorder to its descriptionin the key. Jacobs syndrome a. female with undeveloped ovaries and uterus, unable to undergopuberty, normal intelligence, can live normally with hormonereplacementb. XXY male, can inherit more than two X chromosomesc. male or female, mentally impaired, short stature, flat face, stubbyfingers, large tongue, simian palm creased. XXX or XXXX femalee. caused by nondisjunction during spermatogenesis
- AaBbCcDc 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,…Children with this condition has the following features: wide or web-like neck; low-set ears; broad chest with widely spaced nipples; high, narrow roof of the mouth (palate); arms that turn outward at the elbows; fingernails and toenails that are narrow and turned upward; swelling of the hands and feet, especially at birth; slightly smaller than average height at birth; slowed growth; and cardiac defects. The statement applies to Turner syndrome only The statement applies to Down syndrome only The statement applies to both Turner syndrome and Down syndrome The statement applies to neither Turner syndrome nor Down syndromeA male presenting with clinical features as greater height, poor coordination, less body hair, breast growth and seems less interest in sex. He is also facing difficulty in speech. What your knowledge depicts that he is suffering from which genetic disease.
