Summary A kindred is described with a probably new inherited syndrome, involving bilateral congenital hip dysplasia with coxa vara, patella aplasia and tarsal synostosis. This association is probably inherited as an incomplete dominant trait, apparently as a result of a new mutation. In this case a single pleiotropic gene might be held responsible for the multiple skeletal defects. From a bibliographical review, it may be concluded that the nosological association of these multiple defects has never been published so far.
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Goeminne et al. (1970) studied this question.
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