Congenital Vascular Tortuosity in DiGeorge Syndrome Mimicking Significant Retinopathy of Prematurity

Archives of Ophthalmology

Volumn 122, Issue 1, 2004, Pages 132-133

  Hill, Vivian E ^a   Pietucha, Shamek ^a   Ells, Anna L ^a,b  

^a Alberta Children's Hospital ^*

^b ALBERTA CHILDREN'S HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; DIGEORGE SYNDROME; DISEASE COURSE; DISEASE SEVERITY; DUODENUM ATRESIA; FALLOT TETRALOGY; HUMAN; INFANT; PRIORITY JOURNAL; RETINA BLOOD VESSEL; RETROLENTAL FIBROPLASIA;

DIAGNOSIS, DIFFERENTIAL; DIGEORGE SYNDROME; HUMANS; INFANT, NEWBORN; INTESTINAL ATRESIA; MALE; RETINAL VESSELS; RETINOPATHY OF PREMATURITY; TETRALOGY OF FALLOT;

EID: 0347355037     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.122.1.132     Document Type: Article

References (1)

1. McDonald-McGinn D, Kirschner R, Goldmuntz E, et al. The Philadelphia story: 22q11.2 deletion: report on 250 patients. Genet Couns. 1999;10:11-24.