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  1. Home
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  3. Research By Disease

Disease: Cote Katsantoni syndrome

  • A syndrome of skeletal dysplasia, joint laxity, and mental retardation
  • Another case of Marden-Walker syndrome
  • Ectodermal dysplasia, osteosclerosis, atrial septal defect, malabsorption, neutropenia, growth, and mental retardation: the Cote-Katsantoni syndrome?
  • New syndrome of trichodermal defect and mental retardation
  • Osteosclerosis and ectodermal dysplasia
  • The cytogenetic and clinical implications of a ring chromosome 2
  • The G syndrome of dysphagia, ocular hypertelorism and hypospadias
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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