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  3. Research By Disease

Disease: Teebi Naguib Al Awadi syndrome

  • Brachmann-de Lange syndrome in sibs
  • Down syndrome in Kuwait
  • Familial uterine hernia syndrome: report of an Arab family with four affected males
  • Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle East
  • Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome?
  • Intestinal malformations and Down's syndrome in Arabs
  • Multiple pterygium syndrome in five Arab sibs
  • New autosomal recessive faciodigitogenital syndrome
  • Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females
  • Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome
  • Ullrich-Turner syndrome in monozygotic twins
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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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