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J Med Genet. 1991 April; 28(4): 277–279.
PMCID: PMC1016833

Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.

Abstract

Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Saal HM, Greenstein RM, Weinbaum PJ, Poole AE. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies. Am J Med Genet. 1988 Jul;30(3):709–718. [PubMed]
  • Thompson EM, Winter RM. A child with sclerocornea, short limbs, short stature, and distinct facial appearance. Am J Med Genet. 1988 Jul;30(3):719–724. [PubMed]
  • Kivlin JD, Fineman RM, Crandall AS, Olson RJ. Peters' anomaly as a consequence of genetic and nongenetic syndromes. Arch Ophthalmol. 1986 Jan;104(1):61–64. [PubMed]
  • van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers EM. Peters'-plus: a new syndrome. Ophthalmic Paediatr Genet. 1984 Dec;4(3):141–145. [PubMed]
  • Butler MG, Wadlington WB. Robinow syndrome: report of two patients and review of literature. Clin Genet. 1987 Feb;31(2):77–85. [PubMed]

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