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  1. Home
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  3. Research By Disease

Disease: Rodini Richieri Costa syndrome

  • Amniotic bands and the EEC syndrome
  • Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly
  • Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome
  • Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of Goltz-Gorlin syndrome versus EEC syndrome
  • Ectrodactyly, cleft lip/palate syndrome
  • EEC syndrome: report on 20 new patients, clinical and genetic considerations
  • Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents
  • Newly recognized blepharofacioskeletal syndrome
  • Rapp-Hodgkin syndrome: report of a Brazilian family
  • Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients
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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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