Table 1

Clinical and molecular data in the RHS and EEC families

FamilyPatientGenderDiagnosisClinical signsMutation
RHS, Rapp–Hodgkin syndrome; AEC, ankyloblepharon-ectodermal dysplasia-cleft; EEC, ectodermal dysplasia, ectrodactyly, cleft lip / palate; E, ectodermal dysplasia (anhidrosis, no tears, sparse hair, pili torti / canaliculi, tooth hypoplasia, dysplastic nails); C, cleft; S, syndactyly.
AI-2FemaleRHS or AECC palate, E, slight ankyloblepharon on right eye1859 Del A
AII-1FemaleRHSE1859 Del A
AII-3FemaleRHSC lip/palate, E1859 Del A
BII-5FemaleEECBilateral C lip/palate, left hand S IV/V and absent II/III, right hand S II/V with absent III/IV and clinodactyly I, both feet S III/IV and absent IIR279C
BIII-5MaleEECC lip/palate, obstructed lacrimal ducts, left hand S I/II and absent III, right hand S I/II, left foot S III/IV and absent II, right foot absent II/IIIR279C
CI-2FemaleEECBilateral C lip/palate, sparse eye lashes and eyebrows, obstructed lacrimal ducts, bilateral clinodactyly V, hypoplastic nailsR304Q
CII-1FemaleEECC lip/palate, hypoplastic nails, sparse hair, obstructed lacrimal ducts, right hand preaxial polydactyly, left foot postaxial polydactyly, right foot cutaneous S II/IIIR304Q
CII-2FemaleEECBilateral C, hypoplastic nails, obstructed lacrimal ducts, right hand short distal phalanges III/IV, preaxial polydactyly, left hand absent distal phalanges, right foot cutaneous S III/IV, left foot preaxial polydactylyR304Q
CII-3MaleEECBilateral C lip/palate, hypoplastic nails, obstructed lacrimal ducts, right hand cutaneous S II/III and IV/VR304Q
CII-4MaleEECBilateral C lip/palate, hypoplastic nails, obstructed lacrimal ducts, bilateral hand and foot ectrodactyly, left hand cutaneous SI/II and IV/V, bilateral foot rudimentary II and III and cutaneous S III/IVR304Q