Trio-WES revealed that the fetus carried a compound heterozygous variant, c.1778G > A (p.Ser593Asn) and c.11352C > A (p.Phe3784Leu), in DNAH11, associated with PCD type 7, with or without SI (OMIM 611884)30, as well as another compound heterozygous variant, c.928 T > C (p.Cys310Arg) and c.814_815del (p.Leu272Valfs*66), in PEX10, related to peroxisome biogenesis disorder 6A (Zellweger) (OMIM 614870) and 6 B (OMIM 614871), inherited from the mother and father, respectively. Here, PEX10 is linked to Peroxisome biogenesis disorder-Zellweger syndrome spectrum.