Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency

To present previously undescribed vitreoretinal findings similar to severe retinopathy of prematurity (ROP) in two siblings (daughter and son) with a thrombophilic disorder, compound heterozygous protein S (PS) deficiency. Family genotype study and literature review. Two unrelated heterozygous PS-de...

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Veröffentlicht in:	Ophthalmology (Rochester, Minn.) Minn.), 1999-08, Vol.106 (8), p.1525-1530
Hauptverfasser:	Mintz-Hittner, Helen A, Miyashiro, Michael J, Knight-Nanan, Donna M, O’Malley, Ronan E, Marlar, Richard A
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Electroretinography Evoked Potentials, Visual Female Gestational Age Heterozygote Humans Infant, Newborn Laser Therapy Lens, Crystalline - surgery Male Medical sciences Ophthalmology Orbit diseases Pedigree Protein S - metabolism Protein S Deficiency - blood Protein S Deficiency - complications Protein S Deficiency - genetics Protein S Deficiency - physiopathology Retina - pathology Retina - physiopathology Retinal Neovascularization - etiology Retinal Neovascularization - pathology Retinal Neovascularization - surgery Retinopathy of Prematurity - blood Retinopathy of Prematurity - etiology Retinopathy of Prematurity - pathology Retinopathy of Prematurity - physiopathology Visual Acuity Vitrectomy Vitreous Body - pathology
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