Wyburn-Mason Syndrome - Symptoms, Causes, Treatment | NORD
2024年9月17日 · Wyburn-Mason syndrome is a rare nonhereditary disorder that is present at birth (congenital). Affected infants have arteriovenous malformations (AVMs), which are developmental abnormalities affecting the blood vessels, specifically the …
Wyburn-Mason Syndrome - StatPearls - NCBI Bookshelf
2023年6月26日 · Wyburn-Mason syndrome (WMS), also known as racemose angioma, is a congenital nonhereditary neurocutaneous syndrome or phakomatoses that presents with multiple arteriovenous malformations (AVM). WMS has varied phenotypical expressions but predominantly affects the face and brain.
Wyburn-Mason syndrome | About the Disease | GARD - Genetic …
Wyburn Mason's syndrome is a condition in which blood vessels do not form correctly in both the retina of one eye and a part of the brain. These malformed blood vessels are called arteriovenous malformations (AVM). Wyburn Mason's syndrome is present from birth (congenital) and the cause is unknown.
Ocular Manifestations of Wyburn-Mason Syndrome - EyeWiki
Wyburn-Mason Syndrome is characterized by the presence of AVMs that vary in size and location. These lesions are direct artery-to-vein communications without a capillary system in between to mitigate the high-flow arterial blood.
Bonnet–Dechaume–Blanc syndrome - Wikipedia
Bonnet–Dechaume–Blanc syndrome, also known as Wyburn-Mason syndrome, is a rare congenital disorder characterized by arteriovenous malformations of the brain, retina or facial nevi. [1] The syndrome has a number of possible symptoms and can, more rarely, affect the skin, bones, kidneys, muscles, and gastrointestinal tract. [2]
Orphanet: Wyburn-Mason syndrome
Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterized by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex.
Wyburn-Mason Syndrome: Background, Pathophysiology, Epidemiology - Medscape
2023年2月16日 · Wyburn-Mason syndrome (WMS), also known as Bonnet-Dechaume-Blanc syndrome or retinoencephalofacial angiomatosis, is a rare nonhereditary congenital phakomatosis characterized by...
Wyburn-Mason Syndrome: A Narrative Review - PubMed
2024年8月28日 · Wyburn-Mason syndrome is a rare congenital disorder characterized by arteriovenous malformations (AVMs) in the retina, brain, and occasionally the skin. The syndrome results from embryonic vascular abnormalities and presents with a wide spectrum of clinical manifestations, classified into three grou ….
Wyburn-Mason syndrome – Rare Immunology News
Wyburn Mason's syndrome is a condition in which blood vessels do not form correctly in both the retina of one eye and a part of the brain. These malformed blood vessels are called arteriovenous malformations (AVM). Wyburn Mason's syndrome is present from birth (congenital) and the cause is unknown. Individuals with this condition may have ...
Wyburn-Mason Syndrome - PubMed
2023年6月26日 · Wyburn-Mason syndrome (WMS), also known as racemose angioma, is a congenital nonhereditary neurocutaneous syndrome or phakomatoses that presents with multiple arteriovenous malformations (AVM). WMS has varied phenotypical expressions but predominantly affects the face and brain.
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