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J R Soc Med. 1992 December; 85(12): 759–760.
PMCID: PMC1293768

Richner-Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II)

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Selected References

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  • Goldsmith LA, Kang E, Bienfang DC, Jimbow K, Gerald P, Baden HP. Tyrosinemia with plantar and palmar keratosis and keratitis. J Pediatr. 1973 Nov;83(5):798–805. [PubMed]
  • Natt E, Westphal EM, Toth-Fejel SE, Magenis RE, Buist NR, Rettenmeier R, Scherer G. Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II. Hum Genet. 1987 Dec;77(4):352–358. [PubMed]
  • Rehák A, Selim MM, Yadav G. Richner-Hanhart syndrome (tyrosinaemia-II) (report of four cases without ocular involvement). Br J Dermatol. 1981 Apr;104(4):469–475. [PubMed]
  • Ney D, Bay C, Schneider JA, Kelts D, Nyhan WL. Dietary management of oculocutaneous tyrosinemia in an 11-year-old child. Am J Dis Child. 1983 Oct;137(10):995–1000. [PubMed]
  • Machino H, Miki Y, Kawatsu T, Kida K, Matsuda H. Successful dietary control of tyrosinemia II. J Am Acad Dermatol. 1983 Oct;9(4):533–539. [PubMed]
  • Barr DG, Kirk JM, Laing SC. Outcome in tyrosinaemia type II. Arch Dis Child. 1991 Oct;66(10):1249–1250. [PMC free article] [PubMed]

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