Table 1

Clinical findings and syndrome designations of patients in the study

Family IDGenderCleft typeLimb defectEctodermal defectOtherSyndrome designation
Complete table available (genetics.uiowa.edu).
M, male; F, female; cl/p, cleft lip and palate; bcl/p, bilateral cleft lip and palate; cpo, cleft palate only; lcl/p, left cleft lip and palate; rcl, right cleft lip; AB (amniotic band).
182Mcl/pHemimeliaNoneOcc encephaloceleUnknown
460Mbcl/pNoneNoneSib w ectrodactylyUnknown
494Mbcl/pNoneSparse hairUnknown
599Flcl/pABNone2 cousins: cpoAB
1647McpoNoneNoneSib w ABUnknown
1661Fbcl/pABNoneRelatives: cpoAB
2402Mbcl/pRobert’s synNoneHypotoniaRobert’s syn
3544Fbcl/pABNoneSparse eyebrowsAB
3445Fbcl/pSyndactylyNoneUnknown
4387Fbcl/pABNoneAB
4448Flcl/pABNoneAB
4716Fbcl/pABNoneAB
4939Mlcl/pNoneNoneSibs w ectrodactylyUnknown
4949Mbcl/pABNoneAbd wall defectAB
5084Mbcl/pSyndactylyNoneUnknown
c1108Fbcl/pABSparse eyebrowsAB
c213Mbcl/pEctrodactylyNoneMult congen anomUnknown
19990527FrclABNoneAB
20000121Mrcl/pAB, club footNoneAB
20000141MbclDuplicated thumbNoneUnknown
20000154FlclSyndactylyNoneUnknown
20000191Fbcl/pSyndactyly footSkin tagsUnknown
20000425Fbcl/pABSparse eyebrowsAB
20000498FnoneABAnkyloglossiaUnknown
20000505Mlcl/pDigital ampNoneAB
20000870FcpoHemimeliaNoneAB
20000958Mlcl/pABNoneAB
20001021Mbcl/pABAB
c77Mbcl/pNoneDent anomAnkyloblepharonHay-Wells
699Mbcl/pEctrodactylyNoneAccessory boneUnknown