| Literature DB >> 11273483 |
S K Singh1, S K Bhadada, R Singh, S K Sinha, S K Singh1, J K Agrawal.
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.Entities:
Mesh：
Year: 2000 PMID： 11273483
Source DB: PubMed Journal: J Assoc Physicians India ISSN： 0004-5772