{"orpha":156230,"name":"OBSOLETE: Facial arteriovenous malformation","type":"Clinical group","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Peripheral fast-flow vascular malformation or fistula","url":"https://raremap.alftech.space/d/ORPHA-156230/","orphanet_url":"https://www.orpha.net/en/disease/detail/156230","names":{"fr":{"name":"OBSOLETE : Malformation artérioveineuse faciale"},"de":{"name":"OBSOLET: Arteriovenöse Fehlbildung des Gesichts"},"es":{"name":"OBSOLETO: Malformación arteriovenosa facial"},"it":{"name":"OBSOLETO: Malformazione facciale arterovenosa"},"nl":{"name":"OBSOLEET: Faciale arterioveneuze malformatie"},"pt":{"name":"OBSOLETO: Malformação facial arteriovenosa"},"pl":{"name":"NIEAKTUALNE: Malformacja tętniczo-żylna twarzy"},"cs":{"name":"NEAKTUÁLNÍ: Faciální arteriovenózní malformace"},"uk":{"name":"Артеріовенозна мальформація обличчя","definition":"Facial arteriovenous malformation is a rare vascular anomaly characterized by abnormal communication between arteries and veins, bypassing the capillary bed, located in the facial area. Lesions may be asymptomatic or may manifest with pain, ulceration, pulsation, tinnitus, minor bleeding or potentially life-threatening hemorrhage, blurred vision, impaired hearing, headache, paresthesia, enlargement of facial bones with intraosseous lesions, intraosseous hemangiomas, and speech, breathing and swallowing difficulties, as well as neuropathy."},"zh":{"name":"面部动静脉畸形","definition":"面部动静脉畸形是一种罕见的血管异常，其特征是位于面部的血管与静脉之间连接异常，绕过毛细血管床。病变可能无症状，也可能表现为疼痛、溃疡、搏动、耳鸣、小出血或可能危及生命的出血、视力模糊、听力受损、头痛、感觉异常、伴骨内病变的面骨增大、骨内血管瘤和言语、呼吸、吞咽困难，以及神经病变。"},"tr":{"name":"Yüz arteriyovenöz malformasyonu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":707944,"name":"Peripheral fast-flow vascular malformation"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}