Fundus albipunctatus-like lesions in juvenile retinoschisis.
نویسندگان
چکیده
1 Sonoda T, Hashimoto H, Enjoji M. Juvenile xanthogranuloma: clinicopathological analysis and immnunohistochemical study of 57 patients. Cancer 1985; 56: 2280-6. 2 Zimmerman LE. Ocular lesions of juvenile xanthogranuloma. AmJI Ophthalmol 1965; 60: 1011-35. 3 Collum LMT, Mullaney J. Adult limbal xanthogranuloma. BrJ Ophthalmol 1984; 68: 360-3. 4 Lewis JR, Drummond GT, Mielke BW, Hassard DT, Astle WF. Juvenile xanthogranuloma of the corneo-scleral limbus. CanJ Ophthalmol 1990; 25: 351-4. 5 Collum LM, Power WJ, Mullaney J, Farrell M. Limbal xanthogranuloma. J Paediatr Ophthalmol Strabismus 1991; 28: 157-9. 6 Kaufman JG, Driebe WT, Hamed LM, Margo CE. Juvenile xanthogranuloma of the corneo-scleral limbus. Ophthalmic Surg 1993; 24: 428-30.
منابع مشابه
Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis
PURPOSE To determine clinical phenotypes, examine the age dependency of X-linked juvenile retinoschisis (XLRS), and identify mutations in the retinoschisis1 gene (RS1) in 13 Hungarian (Caucasian) families with this disease. METHODS This study included 72 members in 13 families. Complete ophthalmological examinations, including optical coherence tomography (OCT) and full-field and multifocal e...
متن کاملAssessment of Spectral-Domain Optical Coherence Tomography Findings in Three Cases of X-Linked Juvenile Retinoschisis in the Same Family
X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by splitting of the neurosensory retina. On fundus examination, the macula often has a spoke wheel appearance with foveal cystic lesions, and separation of the retinal layers is typical on spectral-domain optical coherence tomography (SD-OCT). Patients with XLRS can exhibit different clinical course...
متن کاملYoung monozygotic twin sisters with fundus albipunctatus and cone dystrophy.
OBJECTIVE To describe young monozygotic twin sisters with fundus albipunctatus (a type of autosomal recessive stationary night blindness caused by mutations of the 11-cis retinol dehydrogenase gene [RDH5]) associated with cone dystrophy, previously reported in elderly men. METHODS Ophthalmologic examinations were performed, and the RDH5 gene was analyzed by direct genomic sequencing. RESULT...
متن کاملMutational Screening of RS1 gene in X-linked Retinoschisis in an South Indian Family
Purpose: To screen XLRS1 gene for genetic mutations and describe the ocular phenotypes in an X-Linked retinoschisis family. Methods: Ophthalmic examination, including best-corrected visual acuity, fundus photography, Ocular Coherence Tomography/Scanning Laser Ophthalmoscopy (OCT/SLO) and full-field Electroretinography (ERG) was performed in the family. Pedigree was obtained and peripheral blood...
متن کاملInfantile Vitreous Hemorrhage as the Initial Presentation of X-linked Juvenile Retinoschisis
The authors report two cases of X-linked juvenile retinoschisis (XLRS) manifested as bilateral vitreous hemorrhage as early as in an 1-month-old infant and in a 3-month-old infant. The one-month-old male infant showed massive bilateral vitreous hemorrhage. During vitrectomy, thin membrane representing an inner part of schisis cavity was excised and intraschisis hemorrhage was evacuated. As intr...
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ورودعنوان ژورنال:
- The British journal of ophthalmology
دوره 78 8 شماره
صفحات -
تاریخ انتشار 1994