J Med Genet. 1991 Apr;28(4):277-9.

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

de Almeida JC, Reis DF, Llerena Júnior J, Barbosa Neto J, Pontes RL, Middleton S, Telles LF.

Source

Centro de Genética Médica, Instituto Fernandes Figueira, Rio de Janeiro, Brazil.

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.

PMID:: 1856836; [PubMed - indexed for MEDLINE]
PMCID:: PMC1016833

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Peters' plus syndrome. [Am J Med Genet. 1993]
Peters' plus syndrome.
de Almeida JC, Llerena Júnior JC. Am J Med Genet. 1993 Aug 1; 47(1):125.
Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance. [Clin Dysmorphol. 1993]
Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
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Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers.
Boel M, Timmermans J, Emmery L, Dralands G, Fryns JP, Van den Berghe H. Hum Genet. 1979 Oct 1; 51(2):237-40.
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Maillette de Buy Wenniger-Prick LJ, Hennekam RC. Ann Genet. 2002 Apr-Jun; 45(2):97-103.

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