Abstract
Introduction: Robinow syndrome is a rare inherited disorder. It was described by Robinow in 1969 as a syndrome of characteristic facies, micropenis, cryptorchidism in the male and mesomelic limb shortening1. The characteristic facial appearences (foetal face) are frontal bossing, macrocephaly, hypertelorism, wide palpebral fissures with downward slanting, short upturned broad nose with anteverted nares, hyperplastic alveolar ridges, long philtrum, small chin and triangular mouth with downward angles. In addition, hypoplastic genitalia, nevus ...
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