Ann Genet. 2002 Apr-Jun;45(2):97-103.

The Peters' plus syndrome: a review.

Maillette de Buy Wenniger-Prick LJ, Hennekam RC.

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Department of Ophthalmology, Academic Medical Centre, University of Amsterdam, Meibergdreef 15, 1105 AZ, Amsterdam, The Netherlands.

Abstract

Peters' plus syndrome is an infrequently described entity that combines anomalies in the anterior chamber of the eye with other multiple congenital anomalies, and a developmental delay. Major symptoms are extremely variable anterior chamber anomalies, cupid bow of the upper lip, cleft lip and palate, short stature, broad hands and feet, and variable mental delay. The syndrome follows an autosomal recessive pattern of inheritance. The etiology is unknown, but may involve abnormal neural crest development. A review of the pertinent literature is provided.

PMID:: 12119218; [PubMed - indexed for MEDLINE]

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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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Cited by 6 PubMed Central articles

Anterior segment dysgenesis in a child with factor VII deficiency. [Clin Ophthalmol. 2007]
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Beby F, Meunier S, Cochat P, Roche O, Aptel F, Burillon C, Denis P. Clin Ophthalmol. 2007 Sep; 1(3):335-7.
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome. [Am J Med Genet A. 2009]
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome.
Haldeman-Englert CR, Naeem T, Geiger EA, Warnock A, Feret H, Ciano M, Davidson SL, Deardorff MA, Zackai EH, Shaikh TH. Am J Med Genet A. 2009 Aug; 149A(8):1842-5.
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Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-beta2 signaling.
Iwao K, Inatani M, Matsumoto Y, Ogata-Iwao M, Takihara Y, Irie F, Yamaguchi Y, Okinami S, Tanihara H. J Clin Invest. 2009 Jul; 119(7):1997-2008. Epub 2009 Jun 8.

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