Step 1: Zellweger syndrome, also called cerebrohepatorenal syndrome, is a rare congenital disorder.
Step 2: It is characterized by the reduction or absence of functional peroxisomes in the cells, so option (c) is correct.
Step 3: Loss of peroxisomes impairs very long chain fatty acid breakdown and plasmalogen synthesis, leading to impaired neuronal migration, abnormal neuronal positioning, and disturbed brain development.
Step 4: Affected individuals also show reduced CNS myelin (hypomyelination). Lysosomal defects cause storage diseases, mitochondrial defects cause myopathies and encephalopathies, and nuclear loss is incompatible with cell life, so these distractors are wrong.