Solitary retinal capillary hemangioma: Hereditary (von Hippel-Lindau disease) or nonhereditary?

Archives of Ophthalmology

Volumn 119, Issue 2, 2001, Pages 232-234

  Singh, A D ^a   Shields, J A ^a   Shields, C L ^a  

^a WILLS EYE HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGE; ARTICLE; CAPILLARY HEMANGIOMA; CHILD; CONTROLLED STUDY; GENETIC SCREENING; HUMAN; MATHEMATICAL ANALYSIS; PENETRANCE; PRIORITY JOURNAL; PROBABILITY; RETINA TUMOR; RISK ASSESSMENT; THEORY; TREATMENT PLANNING; VON HIPPEL LINDAU DISEASE;

ADOLESCENT; ADULT; AGE FACTORS; AGED; BAYES THEOREM; CHILD; CHILD, PRESCHOOL; HEMANGIOMA, CAPILLARY; HIPPEL-LINDAU DISEASE; HUMANS; INFANT; MIDDLE AGED; PREVALENCE; PROBABILITY; RETINAL NEOPLASMS; RISK FACTORS;

EID: 0035125156     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (28)

1. Aneurysma arterio-venosum retinae
2. Two cases, brother and sister, with peculiar vascular new growth, probably primarily retinal, affecting both eyes
3. Uber eine sehr seltene Erkrankung der netzhaut
4. Forms of retinal disease with massive exudation
5. Zur Frage der angiomatosis retinae und ihrer hirnkomplikationen
6. Lindau's disease
7. Clinical features and natural history of von Hippel-Lindau disease
8. Von Hippel Lindau disease in a large British family: Clinicopathological features and recommendations for screening and following
9. Basic criteria for clinical diagnosis and genetic counseling in von Hippel Lindau syndrome
10. Von Hippel-Lindau disease: A genetic study
11. Clinical features and molecular genetics of von Hippel-Lindau disease
12. Mutation and cancer: Statistical study of retinoblastoma
13. Identification of the von Hippel-Lindau disease tumor suppressor gene
14. Von Hippel-Lindau disease: Genetic, clinical and imaging features
15. Improved detections of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
16. Germline mutations in the yon Hippel-Lindau disease (VHL) gene in the families from North America, Europe, and Japan
17. The two stage mutation model in retinal hemangioblastoma
18. Von Hippel-Lindau disease
19. Clinical and pathological manifestations in nine families with 50 affected members
20. Von Hippel Lindau disease affecting 43 members of a single kindred
21. Early identification of retinal angiomas in a large kindred with von Hippel Lindau disease
22. VHL gene deletion and enhanced VEGF gene expression detected in the stromal cells of retinal angioma
23. A clinical and molecular genetic analysis of solitary ocular angioma
24. Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation
25. Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene
26. Genetic testing for susceptibility to adult-onset cancer: The process and content of informed consent
27. Risk of multisystem disease in isolated ocular angioma