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  3. Research By Disease

Disease: Ramer Ladda syndrome

  • A case of failure to correct humerus-radius synostosis and thumb hypoplasia
  • Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome
  • Congenital humeroradial synostosis with other synostotic anomalies
  • Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome
  • Identical twins with Weissenbacher-Zweymüller syndrome and neural tube defect
  • Marden-Walker phenotype: spectrum of variability in three infants
  • Multiple pterygium syndrome. An overview
  • Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation
  • Rare case of fracture of the two bones of the forearm in a patient with humerus bifurcation and an ulnar deficiency: humero-radioulnar synostosis
  • Resection Arthroplasty Is a Valuable Strategy for Humeroradial Synostosis - A Case Report
  • Roberts syndrome in an Indian patient with humeroradial synostosis, congenital elbow contractures and a novel homozygous splice variant in ESCO2
  • Two infants with del(3)(p25pter) and a review of previously reported cases
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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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