Matching Pairs AbnormalitiesOnline version Match the descriptions to the abnormality by Jennifer Paris 1 Phenylketonuria (PKU) 2 XYY 3 Turner Syndrome (XO) 4 Sickle-Cell Anemia 5 Duchenne Muscular Dystrophy 6 Huntington's Disease 7 Cystic Fibrosis 8 Down syndrome 9 Klinefelter syndrome (XXY) 10 Albinism 11 Tay Sachs Disease 12 Achondroplasia 13 Triple X Syndrome 14 Hemophilia An X-linked chromosomal disorder caused when all or part of one of the X chromosomes is lost before or soon after conception that affects cognitive functioning and sexual maturation. Infertility and a short stature may be noted. A fatal neurological disorder caused by a dominant gene; onset occurs in middle adulthood When the individual lacks melanin and processes little to no pigment in the skin, hair, and eyes. Vision problems can also occur. A blood disorder caused by a recessive gene that mostly affects African American; deformed blood cells affect the ability of the blood to transport oxygen. An X-linked chromosomal disorder caused when an extra Y chromosome is present. There are few symptoms. They may include being taller than average, acne, and an increased risk of learning problems. An X-linked disorder in which the blood doesn’t clot correctly A genetic disease that affects breathing and digestion due to thick mucus building up in the body, especially the lungs and digestive system An X-linked chromosomal disorder caused when an extra X chromosome is present in the cells of a male due to a random event. Can cause some breast development, infertility, and low levels of testosterone. The most common form of disproportionate short stature. The individual has abnormal bone growth resulting in short stature, disproportionately short arms and legs, short fingers, a large head, and specific facial features. A condition characterized by a third chromosome on the 21st pair. Affected individuals have some degree of intellectual disability, characteristic facial features, often heart defects, and other health problems. An X-linked disorder that causes weakening of the muscles resulting in an inability to move, wasting away, and possible death. A disorder caused by a recessive gene in which children cannot metabolize the amino acid phenylalanine A fatal neurological disorder caused by a recessive gene that primarily afflicts Jews of Eastern European origin. An X-linked chromosomal disorder caused when an extra X chromosome is present. It may result in being taller than average, learning difficulties, decreased muscle tone, seizures, and kidney problems.
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