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Fig. 1 | BMC Medical Genetics

Fig. 1

From: A novel missense in GLI3 possibly affecting one of the zinc finger domains may lead to postaxial synpolydactyly: case report

Fig. 1

The clinical phenotype. a. Family tree of the studied individuals (the individuals included in this study are specified by asterisks). Both hands of the proband’s grandfather were classified as post-axial polydactyly type B (individual II:6). The father’s left hand was classified as post-axial polydactyly type B (individual III:2). The patient’s right hand was classified as post-axial polydactyly, and his left hand had cutaneous webbing between the 3rd and 4th fingers; his left foot had a well-formed digit on the fibular aspect (individual IV:1) (b, c and d)

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