European journal of human genetics : EJHG · 2012
Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: a prospective study.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Reinstein Eyal, Pariani Mitchel, Bannykh Serguei, Rimoin David L, Schievink Wouter I
Аннотация
We aimed to assess the frequency of connective tissue abnormalities among patients with cerebrospinal fluid (CSF) leaks in a prospective study using a large cohort of patients. We enrolled a consecutive group of 50 patients, referred for consultation because of CSF leak. All patients have been carefully examined for the presence of connective tissue abnormalities, and based on findings, patients underwent genetic testing. Ancillary diagnostic studies included echocardiography, eye exam, and histopathological examinations of skin and dura biopsies in selected patients. We identified nine patients with heritable connective tissue disorders, including Marfan syndrome, Ehlers-Danlos syndrome and other unclassified forms. In seven patients, spontaneous CSF leak was the first noted manifestation of the genetic disorder. We conclude that spontaneous CSF leaks are associated with a spectrum of connective tissue abnormalities and may be the first noted clinical presentation of the genetic disorder. We propose that there is a clinical basis for considering spontaneous CSF leak as a clinical manifestation of heritable connective tissue disorders, and we suggest that patients with CSF leaks should be screened for connective tissue and vascular abnormalities.
Предметные рубрики MeSH
AdolescentAdultAgedCerebrospinal Fluid LeakCerebrospinal Fluid RhinorrheaChildCollagen Type IIICollagen Type VConnective TissueConnective Tissue DiseasesFemaleFibrillinsGenetic Diseases, InbornGenetic TestingHumansMaleMicrofilament ProteinsMiddle AgedProspective StudiesProto-Oncogene ProteinsTumor Suppressor Proteins