نتایج جستجو برای: angiomatosis

تعداد نتایج: 735  

Journal: :Neurologia 2017
A I Maraña Pérez M L Ruiz-Falcó Rojas V Puertas Martín J Domínguez Carral I Carreras Sáez A Duat Rodríguez V Sánchez González

INTRODUCTION Sturge-Weber syndrome is a congenital vascular disorder characterised by facial capillary malformation (port-wine stain) associated with venous and capillary malformations in the brain and eye. Neurological symptoms and alterations in other locations may also be observed. OBJECTIVES This study describes the clinical and epidemiological characteristics and different treatments in ...

Journal: :Neurology 2015
Amy Wei Lin Timo Krings

Our patient was worked up for mild developmental delay associated with focal scalp alopecia at age 6, and was diagnosed with encephalocraniocutaneous lipomatosis (also known as Haberland or Fishman syndrome), a rare neurocutaneous syndrome characterized by skin lesions (most commonly focal alopecia with or without underlying lipoma), ocular lesions, and CNS anomalies. CNS anomalies are usually ...

Journal: :International Journal of Surgery Case Reports 2018

Journal: :Ear, nose, & throat journal 1992
S F Freedman R G Amedee T Molony

Von Hippel Lindau disease is a hereditary phakomatosis characterized by congenital angiomatosis of the retina and cerebellum. This autosomal dominant syndrome exhibits variable penetrance and expressivity. Because of the marked clinical variability and sporadic age of onset, members of affected families must be counseled and screening protocols established. It has been recommended that initial ...

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