Hyperphosphatemic familial tumoral calcinosis (HFTC) is a condition characterized by an increase in the levels of phosphate in the blood (hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. Research has described many causes for the condition that results in different patterns of inheritance. Here is what we know of the family members: (no other information is provided) II II IV V VI A) Based on the information presented, what is the most likely mode of inheritance? In own words, explain your reasoning. your B) What are the chances that V-6 and V-7 have an afflicted child? C) What are the chances that VI-9 and VI-10 have a HFTC afflicted child?
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a condition characterized by an increase in the levels of phosphate in the blood (hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. Research has described many causes for the condition that results in different patterns of inheritance. Here is what we know of the family members: (no other information is provided) II II IV V VI A) Based on the information presented, what is the most likely mode of inheritance? In own words, explain your reasoning. your B) What are the chances that V-6 and V-7 have an afflicted child? C) What are the chances that VI-9 and VI-10 have a HFTC afflicted child?
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Transcribed Image Text:Hyperphosphatemic familial tumoral calcinosis (HFTC) is a condition characterized by an increase in the
levels of phosphate in the blood (hyperphosphatemia) and abnormal deposits of phosphate and calcium
(calcinosis) in the body's tissues. Research has described many causes for the condition that results in
different patterns of inheritance.
Here is what we know of the family members: (no other information is provided)
II
II
IV
V
VI
A) Based on the information presented, what is the most likely mode of inheritance? In your
own words, explain your reasoning.
B) What are the chances that V-6 and V-7 have an afflicted child?
C) What are the chances that VI-9 and VI-10 have a HFTC afflicted child?
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