Literature DB >> 2787011

Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn).

U M Mayer1, A A Bialasiewicz.   

Abstract

The ocular findings in a newborn with Peters' anomaly and opacity of the lens led to a search for a chromosomal deletion syndrome, confirmed by DNA autoradiography as a partial monosomy 4, Wolf-Hirschhorn syndrome. The child was followed for 13 months. Multiple physical anomalies were observed including incomplete nasal cleft, cerebellar malformations, congenital heart defects, renal malformations, inguinal hernia, malformations of thumbs and toes. Broad beaked nose, broadened nasal root, epicanthus, defect of the medial half of the eyebrows, right-sided facial hypoplasia were the periocular findings. Bilateral microphthalmos, Peters' anomaly with cataracts, and posterior chambers without evident pathology, were found. If the physical development stays satisfactory, anterior segment reconstructive procedures including lensectomy and corneal grafting may prove successful.

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Year:  1989        PMID: 2787011     DOI: 10.3109/13816818909083777

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  3 in total

1.  Trisomy 4p and ocular defects.

Authors:  I W Lurie; V A Samochvalov
Journal:  Br J Ophthalmol       Date:  1994-05       Impact factor: 4.638

Review 2.  Congenital cavitary optic disc anomaly and Axenfeld's anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature.

Authors:  Mohsin H Ali; Nathalie F Azar; Vinay Aakalu; Felix Y Chau; Javaneh Abbasian; Pete Setabutr; Irene H Maumenee
Journal:  Ophthalmic Genet       Date:  2017-12-04       Impact factor: 1.803

Review 3.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367

  3 in total

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