Hutchinson-Gilford progeria is an exceedingly rare human genetic disorder in which there is very early senility and death, usually from coronary artery disease, at an average age of 13 years. Patients, who look very old even as children, do not live to reproduce. Which of the following statements represents the most likely assumption regarding this disorder?
A) The disease is autosomal dominant.
B) The disorder will increase in frequency in successive generations within a family.
C) The disorder may be due to mutation in a single protein-coding gene.
D) Each patient will have had at least one affected grandparent or parent.
Correct Answer:
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