Persistent hyperplastic primary vitreous: Congenital malformation of the eye

Clinical and Experimental Ophthalmology

Volumn 37, Issue 9, 2009, Pages 884-890

  Shastry, Barkur S ^a  

^a OAKLAND UNIVERSITY   (United States)

Author keywords

Congenital; Gene; Hyaloid; Retina; Vitreous

Indexed keywords

FRIZZLED PROTEIN; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 5; PROTEIN P53; WNT PROTEIN;

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 10Q; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; GENE MUTATION; GENETIC PREDISPOSITION; HUMAN; LENS IMPLANT; NONHUMAN; NORRIE DISEASE; PATHOGENESIS; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; PHENOTYPIC VARIATION; RETROLENTAL FIBROPLASIA; REVIEW; VITREORETINOPATHY;

ANIMALS; DIAGNOSIS, DIFFERENTIAL; DISEASE MODELS, ANIMAL; EYE DISEASES; GENES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; VITREOUS BODY;

EID: 73649140307     PISSN: 14426404     EISSN: 14429071     Source Type: Journal    
DOI: 10.1111/j.1442-9071.2009.02150.x     Document Type: Review

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