
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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List some common sex-linked human diseases and some common autosomal human diseases
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- Genetic disorders Complete the following statements to describe several genetic disorders and their symptoms. Choices can be used more than once. The disorder called causes blue-colored skin, sickle-cell disease osteogenesis imperfecta The disorder called that leads to weakened, brittle bones. causes defective collagen methemoglobinemia autosomal dominant The disorder called causes abnormally thick mucus in the bronchial tubes and pancreatic ducts. autosomal recessive The disorder called leads to progressive cystic fibrosis degeneration of neurons in the brain. alkaptonuria The disorder called causes urine to be black. Huntington disease acer %23 24 & 4 8. 9. e y u < 6arrow_forward1arrow_forwardAccording to the current scientific understanding of the topic, why is our gender identity is NOT a matter of choice?arrow_forward
- List the type of heredity (ie autosomal dominant and recessive, X-linked dominant and recessive, epistasis, polygenic, codominant) for color blindness, ABO Blood types, Rh factor, nail patella syndrome, Fragile X syndrome, Kleinfelter syndrome, Turner syndrome, Trisomy 21, CAIS, albinism, PKU.arrow_forwardWrite 2 paragraphs answering the following questions: What is an intersex condition? How should parents raise their intersex children: as girls, boys or intersex? Would it be better for society to recognize 3 sexes instead of two? Why?arrow_forwardProvide a comprehensive and descriptive listing of a minimum of ten family stressors.arrow_forward
- Describe four (4) signs and symptoms a person would suffer with a UTIarrow_forwardDescribe in words the likely transmission of an autosomal dominant disorder. Include details of the parent’s genotype and subsequent pattern and probability of inheritance of the single gene disorder for the offspring produced and provide an example of an autosomal dominant disorderarrow_forwardwhich genetic disorder fits below description trisomy 13. Affected individuals have Microencephaly, microphthalmia, and most die shortly after birth.arrow_forward
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