{"orpha":141168,"name":"OBSOLETE: Frontonasal arteriovenous malformation","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Peripheral fast-flow vascular malformation or fistula","url":"https://raremap.alftech.space/d/ORPHA-141168/","orphanet_url":"https://www.orpha.net/en/disease/detail/141168","names":{"fr":{"name":"OBSOLETE : Malformation artérioveineuse frontonasale"},"de":{"name":"OBSOLET: Arteriovenöse Fehlbildung, frontonasale"},"es":{"name":"OBSOLETO: Malformación arteriovenosa frontonasal"},"it":{"name":"OBSOLETO: Malformazione arterovenosa frontonasale"},"nl":{"name":"OBSOLEET: Frontonasale arterioveneuze malformatie"},"pt":{"name":"OBSOLETO: Malformação arteriovenosa frontonasal"},"pl":{"name":"NIEAKTUALNE: Malformacja tętniczo-żylna czołowo-nosowa"},"cs":{"name":"NEAKTUÁLNÍ: Frontonazální arteriovenózní malformace"},"uk":{"name":"Фронтоназальна артеріовенозна мальформація","definition":"Frontonasal arteriovenous malformation is a rare vascular anomaly characterized by abnormal communication between arteries and veins, bypassing the capillary bed, located in the frontonasal area. It may present with intermittent nasal bleeding, blurred vision, pustule formation and/or disfigurement. Overlying skin may be of normal appearance or may manifest a red, pulsatile mass with local rise of temperature. Other features may include pain, ulceration, excessive growth and/or congestive heart failure."},"zh":{"name":"额鼻部动静脉畸形","definition":"额鼻动静脉畸形是一种罕见的血管畸形，其特征是额鼻部的动脉和静脉之间连接异常，无毛细血管床连接。可表现为间歇性鼻出血、视力模糊、脓疱形成和/或毁容。表面皮肤可能为正常外观，也可能表现为局部温度升高的红色搏动性肿块。其他特征可能有疼痛、溃疡、过度生长和/或充血性心力衰竭。"},"tr":{"name":"Frontonazal arteriyovenöz malformasyon"}},"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}