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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families

Fig. 2

Clinical features of patients in Family 1 with DA2B (a-h) and Family 2 with mild DA (i-k). a Ulnar deviation and contractures in patient II5. b Camptodactyly and adducted thumbs in patient III1. c Flexed toes and talipes equinovarus in patient II5. d Dysplastic ear and attached ear lobes in patient II5. e Small mouth with limited opening in patient II5. f Downward-slanting palpebral fissures, a small chin, and deep folds in the nasolabial area and forehead in patient II5. g Flexion contracture yielding stiff elbows in patient II5. h Short stature of patient II5 (unaffected II6 [left], 178 cm; patient II5 [right], 156.5 cm). i Camptodactyly and ulnar deviation in patient II5. j Mild contractures of the fingers in patient II2. k X-ray findings of patient III1 in 5 years old indicate camptodactyly and ulnar deviation

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