Macular coloboma in siblings affected by different phenotypes of retinitis pigmentosa

Eye

Volumn 18, Issue 4, 2004, Pages 421-428

  Parmeggiani, F ^a,b,c   Milan, E ^b   Costagliola, C ^a   Giuliano, M ^b   Moro, A ^b   Steindler, P ^b   Sebastiani, A ^a  

^a UNIVERSITY OF FERRARA   (Italy)

^b Camposampiero Hospital   (Italy)

^c NONE   (Italy)

Author keywords

Macular coloboma; Nystagmus; Phenotypic heterogeneity; Retinitis pigmentosa

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; COLOBOMA; COLOR VISION TEST; CONGENITAL NYSTAGMUS; DOCUMENTATION; ELECTRONYSTAGMOGRAPHY; ELECTRORETINOGRAPHY; EYE MOVEMENT DISORDER; FATHER; FEMALE; FLUORESCENCE ANGIOGRAPHY; FOLLOW UP; HUMAN; KERATOMETRY; MALE; ORTHOPTICS; PHENOTYPE; RETINA DISEASE; RETINA MACULA DEGENERATION; RETINITIS PIGMENTOSA; RETROSPECTIVE STUDY; SIBLING; TAPETORETINAL DEGENERATION; VISUAL FIELD; VISUAL IMPAIRMENT; VISUAL SYSTEM EXAMINATION;

EID: 2342486787     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.eye.6700689     Document Type: Article

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