Robinow syndrome.

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Date
2000-08-29
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Abstract
Robinow syndrome is a rare congenital abnormality. It is characterized by mesomelic brachymelia, hemivertebrae, dysmorphic facies, genital hypoplasia, micropenis, clinodactyly, camptodactly, hypoplastic nails and moderate short stature. We are documenting the case on the account of its rarity and additional features.
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Singh SK, Bhadada SK, Singh R, Sinha SK, Singh SK, Agrawal JK. Robinow syndrome. Journal of the Association of Physicians of India. 2000 Aug; 48(8): 836-7
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https://imsear.searo.who.int/handle/123456789/92355
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Journal of the Association of Physicians of India