Genes and phenotypes in vascular malformations
نویسندگان
چکیده
منابع مشابه
vascular malformations in the maxillofacial region
congenital vascular lesions occur most often in children. parents of these children take them to maxillofacial surgeons directly or during the treatment of other complications such as infection or jaw bone disorders. various terms now used are unable to describe the pathogenesis and mechanism of the effect of vascular lesions on growth and development of facial bone. term of hemangioma is used...
متن کاملVascular malformations
1. Venous malformations: congenital venous anomalies pathologically characterised by anomalous veins (thickened and hyalinised walls) separated by normal brain. These anatomically abnormal veins drain normal brain tissue. It is thought that they result from intrauterine ischemic event occurring during the formation of medullary veins resulting in collateral venous drainage. This is the most com...
متن کاملVascular malformations in childhood.
Vascular malformations are inborn errors of vascular embryogenesis present at birth that should be diagnosed in childhood and, when necessary, treated to prevent later complications. The current trend is to classify these lesions according to flow characteristics and the predominant type of vascular channel affected. Given the complexity, and in many cases, the rarity, of vascular malformations...
متن کاملExtracranial vascular malformations (hemangiomas and vascular malformations) in children and adolescents – diagnosis, clinic, and therapy
The field of extracranial vascular anomalies is considered as special focus of pediatric otolaryngology and it has shown a rapid development during the last years. The reason for this interest is finally also due to the global acceptance of the classification introduced by the ISSVA (International Society for the Study of Vascular Anomalies). Hemangiomas are the most frequently observed vascula...
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ژورنال
عنوان ژورنال: Clinical and Experimental Dermatology
سال: 2020
ISSN: 0307-6938,1365-2230
DOI: 10.1111/ced.14513