Autosomal dominante vitreoretinale Dystrophie mit Skelettdysplasie in einer Generation

التفاصيل البيبلوغرافية
العنوان: Autosomal dominante vitreoretinale Dystrophie mit Skelettdysplasie in einer Generation
المؤلفون: G. E. Lang, R. A. Pfeiffer, B. Laudi
المصدر: Klinische Monatsblätter für Augenheilkunde. 198:207-214
بيانات النشر: Georg Thieme Verlag KG, 1991.
سنة النشر: 1991
مصطلحات موضوعية: Retina, Pathology, medicine.medical_specialty, Skeletal anomalies, business.industry, Retinoschisis, Retinal detachment, medicine.disease, Brachyolmia, Ophthalmology, medicine.anatomical_structure, Medicine, Vitreoretinal dystrophy, business, Retinopathy, Retinal hole
الوصف: We report on ten patients of four generations with autosomal dominant vitreoretinal dystrophy with different manifestation. The ophthalmological findings are retinal detachment, retinal holes, retinoschisis, lattice and snowflake degeneration, vitreoretinal adhesions, chorioretinal atrophy and peripheral pigment epithelial changes. Two sisters show growth retardation with skeletal anomalies most likely brachyolmia.
تدمد: 1439-3999
0023-2165
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::81ed395f1ff9f91efa35f74ca2b07610Test
https://doi.org/10.1055/s-2008-1045954Test
رقم الانضمام: edsair.doi...........81ed395f1ff9f91efa35f74ca2b07610
قاعدة البيانات: OpenAIRE