【佳學(xué)基因檢測(cè)】足細(xì)胞足突清除基因檢測(cè)

足細(xì)胞足突清除基因檢測(cè)：

足細(xì)胞足突清除基因檢測(cè)方法評(píng)估: 來(lái)自甘肅省張掖市臨澤縣倪家營(yíng)鄉(xiāng)的鄒加怡（化名）在鞍山市中心醫(yī)院被醫(yī)生診斷為足細(xì)胞足突清除。歸納《 Experimental Nephrology Exp Nephrol》，足細(xì)胞足突清除的出現(xiàn)有多種原因，其中一個(gè)重要的原因是基因突變，這需要通過(guò)基因檢測(cè)來(lái)明確?；蛲蛔円鸬目赡軙?huì)遺傳。

本文關(guān)鍵詞

足,細(xì)胞,足突清除,基因檢測(cè)

人體疾病表征數(shù)據(jù)庫(kù)查詢(xún)

產(chǎn)生足細(xì)胞足突清除醫(yī)師會(huì)懷疑以下疾病類(lèi)型：

怎樣才能診斷正確？

HP:0031266

表型描述

An anomaly of podocyte morphology characterized by the loss of the interdigitating foot process pattern (generally called foot process effacement; FPE). The term FPE designates the loss of the usual interdigitating pattern of foot processes of neighboring podocytes, leading to relatively broad expanses of podocyte processes covering the glomerular basement membrane (GBM). It is widely viewed as a pathological derangement that is associated with leakage of macromolecules such as albumin through the glomerular filtration barrier.