| Question 1: Other signs that may point to FAP are pigmented lesions of the ________ ("CHRPE - congenital hypertrophy of the retinal pigment epithelium"), jaw cysts, sebaceous cysts, and osteomata (benign bone tumors). | |||
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| Question 2: If the blood is not visible, it is still possible for the patient to develop ________ due to gradually developing iron deficiency. | |||
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| Question 3: ________ is possible if a disease-causing mutation is identified in an affected family member; however, prenatal testing for typically adult-onset disorders is uncommon and requires careful genetic counseling. | |||
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| Question 4: However, other tumor-suppressor functions of Apc may be related to cell adherence and ________ organization. | |||
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| Question 5: Various medications are being investigated for slowing malignant degeneration of polyps, most prominently the ________ (NSAIDs). | |||
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| Question 6: When this condition results from mutations in the ________, it is inherited in an autosomal dominant pattern, which means one copy of the altered gene is sufficient to cause the disorder. | |||
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| Question 7: Mutations in the MUTYH gene are inherited in an ________ pattern, which means two copies of the gene must be altered for a person to be affected by the disorder. | |||
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| Question 8: Ultrasound of the abdomen and blood tests evaluating liver function are often performed to rule out ________ to the liver. | |||
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| Question 9: MYH glycosylase fixes these mistakes by base excision repair, such that mutations do not accumulate in the ________ and lead to tumor formation. | |||
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| Question 10: For more information see ________. | |||
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