Becker muscular dystrophy causes
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Sex-Linked Chromosomal Disorders. by April Jones. Rabun County High School, Tiger, Georgia. Primary Learning Outcomes. Students will learn the names, characteristics, and causes of several different sex linked disorders, including muscular dystrophy.
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Both Duchenne muscular dystrophy and Becker muscular dystrophy result from mutations in the DMD gene on the X chromosome. About two-thirds of cases are due to deletion mutations. The severity of the effects of these deletion mutations in the DNA depends in large part on the number of nucleotides deleted in the mRNA (
Causes of Muscular Dystrophy: Common Risk Factors, Genetics, an…
Becker muscular dystrophy is a muscle-wasting condition, caused when a vital muscle protein called dystrophin does not work properly The condition causes muscles to weaken and waste over time, leading to increasingly severe disability and in some cases, life-threatening health problems, as heart and breathing muscles weaken.
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A second type is Becker's muscular dystrophy, which is similar to the Duchenne form of the disease. Approximately three in two hundred thousand people are affected, and it too is found only among males. The major clinical difference is the age of onset. Becker's muscular dystrophy typically first appears in the early teenage years.
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A Collaborative Research Project Based on the California State Standards in Biology Grades 9-12. Claire Carey. Santa Barbara High School. UCSB RET II 2006
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Becker muscular dystrophy is milder. Symptoms do not begin until age 12 or later, and a person with Becker muscular dystrophy often survives into his forties. His muscle cells have an abnormal version of dystrophin that is somewhat effective for keeping muscle cells alive.
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The onset of cardiomyopathy in people with Becker muscular dystrophy is later, usually in early to mid-adulthood. Incidence of Duchenne and Becker muscular dystrophy. Duchenne and Becker muscular dystrophies together affect 1 in 3,500 to 5,000 newborn males. Between 400 and 600 boys in the United States are born with these conditions each year.
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The pedigree shows the occurrence of Becker muscular dystrophy in a family. Becker muscular dystrophy causes muscle weakness. Based on this pedigree, it is . most. reasonable to conclude that Becker muscular dystrophy is which of the following? a polygenic trait. a codominant trait. an autosomal dominant trait. a sex-linked recessive trait ...
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A systematic review and meta-analysis on theepidemiology of Duchenne and Becker muscular dystrophy. 2014;24:482-491. 5 Ciafaloni E, Fox DJ, Pandya S, Westfield CP, Puzhankara S, Romitti PA, et al. Delayed diagnosis in Duchenne muscular dystrophy: data from the muscular dystrophy surveillance, tracking, and research network (MD-STARnet).
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May 04, 2011 · Becker muscular dystrophy causes muscle weakness. Based on this pedigree, it is most reasonable to conclude that Becker muscular dystrophy is which of the following? A. a polygenic trait B. a codominant trait C. a sex-linked recessive trait D. an autosomal dominant trait 24. The mold Aspergillus flavus grows on grain. ...
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