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1.
Am J Ophthalmol ; 136(2): 258-63, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12888047

ABSTRACT

PURPOSE: To investigate outcomes in premature infants with high-risk retinopathy of prematurity and secondary vitreous hemorrhage. DESIGN: Retrospective chart review. METHODS: Patients were selected from a database of infants undergoing retinopathy of prematurity screening from September 1997 to November 1999. Infants with high-risk retinopathy of prematurity (zone I or posterior zone II threshold disease) with and without vitreous hemorrhage were compared. MAIN OUTCOME MEASURES: Final stage of retinopathy of prematurity and short-term structural outcome were assessed. Visual acuity and refraction were measured when possible. RESULTS: Twenty-two eyes of 11 patients (group 1) had high-risk (posterior zone II or zone I threshold) retinopathy of prematurity without vitreous hemorrhage. Group 1 patients had a 91% favorable short-term structural outcome. Eight eyes of five infants developed vitreous hemorrhage with high-risk retinopathy of prematurity (group 2). Group 2 patients had only a 12.5% favorable short-term structural outcome. Seven of eight (87.5%) progressed to stage IVa or IVb retinopathy of prematurity. Six eyes underwent vitreoretinal surgery after a median duration of hemorrhage of 36 +/- 29 days (4-70 days). Three eyes developed stage V detachments and three progressed to phthisical degeneration. Final visual acuity was no light perception in three eyes. CONCLUSION: Vitreous hemorrhage, in association with advanced retinopathy of prematurity, is a poor prognostic sign.


Subject(s)
Retinopathy of Prematurity/complications , Vitreous Hemorrhage/etiology , Birth Weight , Gestational Age , Humans , Infant, Newborn , Prognosis , Refraction, Ocular , Retinal Detachment/etiology , Retinopathy of Prematurity/physiopathology , Retrospective Studies , Risk Factors , Visual Acuity , Vitreous Hemorrhage/physiopathology
2.
J Pediatr Ophthalmol Strabismus ; 41(6): 369-72, 2004.
Article in English | MEDLINE | ID: mdl-15609525

ABSTRACT

We present a case of a child with Kabuki syndrome and jaw-winking ptosis. Kabuki syndrome is rare and consists of a constellation of findings including mental retardation, characteristic oculofacial features, and skeletal abnormalities. The association of Kabuki syndrome and jaw-winking ptosis has not been previously reported.


Subject(s)
Abnormalities, Multiple , Blepharoptosis/congenital , Intellectual Disability/genetics , Mandible/abnormalities , Oculomotor Muscles/innervation , Blepharoptosis/diagnosis , Blepharoptosis/therapy , Blinking , Child , Female , Humans , Mandible/innervation , Syndrome
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