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Original Articles

Can you name this congenital syndrome?

, MD
Pages 207-209 | Published online: 30 Jun 2015

References

  • Laurence JZ, Moon RC. Four cases of retinitis pigmentosa occurring in the same family and accompanied by general imperfection of development. Ophthalmol Rev 1866; 2: 32–41
  • Biedl A. Ein geschwister Paar mit adiposo-genitaler Dystrophie. Dtsch Med Wochenschr 1922; 48: 1630
  • Bardet G. Sur un syndrome d'obésité congénitale avec poly- dactylie et rétinite pigmentaire (contribution à l'étude des formes clinique de l'obésité hypophysaire). Thè se de Paris 1920; 170: 10–7
  • Edwards JA, Sethi PK, Scoma AJ, et al. A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance. Am J Med 1976; 60(l): 23–32
  • Hersh JH, Podruch PE, Weisskopf B. Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome? Birth Defects Orig Artie Ser 1982; 18(3B): 175–82
  • Green JS, Parfrey PS, Harnett JD, et al. The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N Engl J Med 1989; 321 (15): 1002–9
  • Harnett JD, Green JS, Cramer BC, et al. The spectrum of renal disease in Laurence-Moon-Biedl syndrome. N Engl J Med 1988; 319(10): 615–8

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