camptodactyly-taurinuria syndrome https://www.malacards.org/card/camptodactyly_taurinuria_syndrome MEDGEN:1385639 GARD:0001069 camptodactyly taurinuria SCTID:733466005 MESH:C537972 familial streblodactyly with amino-aciduria Orphanet:1325 UMLS:C4518792 camptodactyly with taurinuria Camptodactyly-taurinuria syndrome is a congenital malformation syndrome characterized by the association of a permanent camptodactyly of the fingers with the over excretion of taurine in the urine. Camptodactyly mainly affects the little finger, although any finger may be involved. The disease has been described in 17 affected patients from 4 unrelated families. An autosomal dominant inheritance has been suggested. There have been no further descriptions in the literature since 1966. MONDO:0015272 congenital limb malformation