Answer:
C. Every case of progeria must be caused by a new mutation.
Step-by-step explanation:
Progeria is a rare disease which is caused by the defect in the production of the progerin protein or the lamin A.
The progeria is caused when a mutation on the gene which codes for the lamin A protein occurs. The progerin protein is involved in forming the nuclear lamina and thus maintain the structure of the nucleus. When the nucleus lacks the protein then the nucleus becomes unstable and the cell dies at an early age.
Since the condition is caused by the dominant allele and the baby dies before the sexual stage, therefore, the allele is not transferred and there are no chances that the disease is an inherited disease but by a new mutation in a gene.
Thus, Option-C is correct.