Decode-the-pedigree approach.
First name the inheritance pattern from the diagram, then map it to a disease.
Pedigree clues present:
• Affected individuals are essentially all male (filled squares).
• Disease passes through unaffected carrier females (dotted circles).
• There is no male-to-male transmission (an affected father never passes it to his son).
This combination is diagnostic of X-linked recessive inheritance - affected males inherit the mutant X from carrier mothers, and fathers pass their X only to daughters (who become carriers).
Now test each option for X-linked recessive status:
• Wiskott-Aldrich → X-linked recessive (WAS gene) - MATCH.
• Wilson → autosomal recessive (ATP7B) - both sexes, sibling clustering; no.
• Prader-Willi → genomic imprinting / paternal 15q deletion; not X-linked; no.
• Achondroplasia → autosomal dominant (FGFR3); vertical, male-to-male possible; no.
Only Wiskott-Aldrich fits an X-linked recessive pedigree ($answer = Option\ A$, matching the key).
Memory aid: all-affected-male + carrier-female transmission + no father-to-son = X-linked recessive → here, Wiskott-Aldrich.