Autosomal dominante vitreoretinale Dystrophie mit Skelettdysplasie in einer Generation
العنوان: | Autosomal dominante vitreoretinale Dystrophie mit Skelettdysplasie in einer Generation |
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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 |
تدمد: | 14393999 00232165 |
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