Which of the following conditions is not the result of a chromosomal alteration? O Chronic myelogenous leukemia (CML) O Down syndrome (Trisomy 21) O Turner syndrome O Mosaicism
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- A patient has two parents with Huntington's disease. They may not have inherited this autosomal dominant disorder due to: 1) increased DNA repeats (CAG) during spermatogenesis 2) incomplete penetrance 3) inheriting one recessive allelewhich genetic disorder matches below descriptions. extra 21st chromosome attaches to chromosome 14. Affected individual exhibit epichanthic folds of eyelids, simian crease in palms, and mental retardation. trisomy 18 Affected individuas have an elongated skull, hair lip, cleft palate, rocker-bottom feet. Life expectancy is about 10 weeks. trisomy 21. Affected indiviudals exhibit epicanthic folds of eyelids, protruding tongue, small, low set ears, and retardation.Match the disease with the pattern of inheritance Phenylketonuria Achondroplasia Autosomal Autosomal X-linked X-linked dominant recessive recessive dominant O Y-linked
- 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 SyndromeUsing the karyotype and the disorder charts below, which of the following abnormalities is true for this female? 88 あ8 AK %8 88 XK 88 器器お品 12 15 18 XX XX 19 20 21 22 Disorder Cause Turner Syndrome Patau Syndrome Edward's Syndrome Down Syndrome Triple X Syndrome Monosomy X Trisomy 13 Trisomy 18 Trisomy 21 Trisomy X O Patau Syndrome O Down Syndrome O Turner Syndrome O Triple X Syndrome O Edward's SyndromeYou may include drawings as part of your answers. Explain in detail 2 human chromosomal disorders. What is the chromosomal abnormality? What are the signs, symptoms, and/or resulting syndrome?
- 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,…Given the karyogram below, anSW Is this a male or female? female Do you see any abnormality? Yes 13 Write the karyotype (genetically speaking)|From the powerpoint presentation, choose five (5) terms or concepts pertaining to chromosomal abnormality in the number. Describe each in a sentence. https://www.slideshare.net/farhanali911/chromosomal-abnormalities-33461290
- You met with two parents whose first child has sickle cell anemia. (The parents show no signs of the disease themselves). The mother comes to you in the third month of her second pregnancy, and wants to know if this child will also inherit the disease. As a genetics counselor, you are ready to evaluate this couple’s case by doing the following:1. Determine what the genotype of each parent is. Is this disease autosomal or sex-linked? Dominant or recessive?Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked reccessive inheritance, sex-linked dominay inheritance or y-linked inheritance.Please help me with the following question: Von Willebrand disease is an inherited bleeding disorder. People with von Willebrand disease take a much longer period for blood to clot/stop than others. von Willebrand disease is either inherited in an autosomal dominant pattern or in an autosomal recessive pattern. Question: what is the genotype of the disorder? what are the phenotypic effects of the disorder? What is happening with the DNA to cause the phenotypic effects?