Hereditary hemorrhagic telangiectasia;Maladie de Rendu-Osler

Revue du Praticien

Volumn 59, Issue 7, 2009, Pages 899-903

  Plauchu, Henri ^a   Dupuis Girod, Sophie ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA;

ANEMIA; AUTOSOMAL DOMINANT INHERITANCE; BRAIN ABSCESS; BRAIN ARTERIOVENOUS MALFORMATION; BRAIN HEMORRHAGE; EPISTAXIS; FRANCE; HUMAN; NEUROLOGICAL COMPLICATION; PENETRANCE; PREVALENCE; PULMONARY ARTERIOVENOUS FISTULA; RENDU OSLER WEBER DISEASE; REVIEW; TELANGIECTASIA; TRANSIENT ISCHEMIC ATTACK;

HUMANS; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 70349748496     PISSN: 00352640     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (13)

1. Henri Rendu (1844-1902). Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux. Gaz Hop Paris 1896;135:1322-1326
2. Plauchu H, de Chadarevian JP, Bideau A, Robert JM. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet 1989;32:291-297 (Pubitemid 19146524)
3. Bideau A, Plauchu H, Brunet G, Robert J. Epidemiological investigation of Rendu-Osler disease In France: its geographical distribution and prevalence. Popul 1989;44:3-22.
4. Plauchu H. Maladie de Rendu-Osler: Quelle surveillance? Rev Prat Med Gen 2004;18:333-336
5. Cottin V, Plauchu H, Bayle JY, Barthelet M, Revel D, Cordier JF. Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. Am J Respir Crit Care Med 2004;169:994-1000. (Pubitemid 38543636)
6. Cottin V, Chinet T, Lavole A, et al. Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: a series of 126 patients. Medicine (Baltimore) 2007;86:1-17. (Pubitemid 46104915)
7. Fulbright RK, Chaloupka JC, Putman CM, et al. MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations. AJNR Am J Neuroradiol 1998;19:477-484 (Pubitemid 30422752)
8. Bernard G, Mion F, Henry L, Plauchu H, Paliard P. Hepatic involvement in hereditary hemorrhagic telangiectasia: clinical, radiological, and hemodynamic studies of 11 cases. Gastroenterology 1993;105:482-487 (Pubitemid 23213534)
9. Buscarini E, Buscarini L, Civardi G, Arruzzoli S, Bossalini G, Plantanida M. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings. AJR Am J Roentgenol 1994;163:1105-1110 (Pubitemid 24355700)
10. Buscarini E, Plauchu H, Garcia Tsao G, et al. Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations. Liver Int 2006;26:1040-1046 (Pubitemid 44541744)
11. Abdalla SA, Geisthoff UW, Bonneau D, et al. Visceral manifestations in hereditary haemorrhagic telangiectasia type 2. J Med Genet 2003;40:494-502. (Pubitemid 36843071)
12. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-67 (Pubitemid 30127562)
13. Babin E, Borsik M, Braccard S, et al. Indications et stratégies thérapeutiques des épistaxis dans la maladie de Rendu Osler. Rev Laryngol Otol Rhinol (Bord) 2005;126:43-48 (Pubitemid 40979432)