TY - JOUR
T1 - Tibial hypoplasia with a bifid tibia
T2 - an unclassified tibial hemimelia
AU - Shah, Krupa
AU - Shah, Hitesh
N1 - Publisher Copyright:
2016 BMJ Publishing Group Ltd.
PY - 2016/8/16
Y1 - 2016/8/16
N2 - Tibial hemimelia is a rare congenital limb deficiency which is characterised by a hypoplastic/aplastic tibia. It actually represents a spectrum of anomalies, ranging from mild hypoplasia of the tibia to total absence of the tibia. Several classifications based on radiological description exist in the literature. The tibial hemimelia is usually described with preaxial mirror polydactyly, split hand/foot syndrome-ectrodactyly, polydactyly-triphalangeal thumb syndrome (Werner syndrome) and micromelia-trigonal brachycephaly syndrome. We describe a child with unclassified tibial hemimelia. The child had right incomplete tibial hemimelia with bifid tibia, left complete tibial hemimelia, bilateral split hands and left split foot. This is the first report of the bifid tibia in the literature.
AB - Tibial hemimelia is a rare congenital limb deficiency which is characterised by a hypoplastic/aplastic tibia. It actually represents a spectrum of anomalies, ranging from mild hypoplasia of the tibia to total absence of the tibia. Several classifications based on radiological description exist in the literature. The tibial hemimelia is usually described with preaxial mirror polydactyly, split hand/foot syndrome-ectrodactyly, polydactyly-triphalangeal thumb syndrome (Werner syndrome) and micromelia-trigonal brachycephaly syndrome. We describe a child with unclassified tibial hemimelia. The child had right incomplete tibial hemimelia with bifid tibia, left complete tibial hemimelia, bilateral split hands and left split foot. This is the first report of the bifid tibia in the literature.
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U2 - 10.1136/bcr-2016-216622
DO - 10.1136/bcr-2016-216622
M3 - Article
C2 - 27530878
AN - SCOPUS:85013770984
SN - 1757-790X
VL - 2016
JO - BMJ Case Reports
JF - BMJ Case Reports
ER -