Hereditary persistence of alpha-fetoprotein (HPAF P): review of the literature.

Hereditary persistence of alpha-fetoprotein (HPAF P): review of the literature.
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甲胎蛋白(HPAF P)的遗传性持续性:文献综述。

DOI:
--
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发表时间:
2010
影响因子:
--
通讯作者:
M. Lock
M. Lock
中科院分区:
医学4区
文献类型:
--
作者:
A. C. Houwert;J. Giltay;E. Lentjes;M. Lock

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相似文献

甲胎蛋白(AFP)血清水平在几种临床情况下都会升高,从非病理情况到恶性肿瘤。遗传性甲胎蛋白持续性(HPAFP)是一种罕见的甲胎蛋白水平升高的良性疾病。HPAFP被描述为一种良性的常染色体显性遗传疾病,与任何临床残疾或其他症状无关。在过去的28年里,只有19个家系被描述;由于对HPAFP的不熟悉,AFP水平升高从未被归因于HPAFP。然而,未诊断的HPAFP可能导致不适当和不必要的治疗决定。因此,对于AFP水平升高原因不明的患者,尤其是有泌尿系统疾病的患者,应考虑HPAFP。
Alpha-fetoprotein (AFP) serum levels are raised in several clinical conditions, ranging from non-pathological conditions to malignancies. Hereditary persistence of alpha-fetoprotein (HPAFP) is a rare benign disorder with elevated AFP levels. HPAFP is described as a benign autosomal dominantly inherited condition which is not associated with any clinical disability or additional symptoms. In the past 28 years, only 19 families have been described; due to this unfamiliarity with HPAFP, elevated AFP levels are never attributed to HPAFP. However, undiagnosed HPAFP can result in inappropriate and unnecessary treatment decisions. Therefore, HPAFP should be taken into consideration in patients with unexplained elevated AFP levels, and especially in patients with urological disorders.
人类 4 号染色体 q11-22 内与进化相关的血清白蛋白和甲胎蛋白基因的连锁。
DOI: --
发表时间: 1983
影响因子: 9.8
作者:
Harper,ME;Dugaiczyk,A
通讯作者: Dugaiczyk,A
人类甲胎蛋白基因的染色体结构和定位。
DOI: 10.1111/j.1749-6632.1983.tb32842.x
发表时间: 1983
影响因子: 5.2
作者:
Minghetti,PP;Harper,ME;Alpert,E;Dugaiczyk,A
通讯作者: Dugaiczyk,A
DOI: 10.1097/00000441-199203000-00004
发表时间: 1992-03-01
影响因子: 3.1
作者:
BALL, D;ROSE, E;ALPERT, E
通讯作者: ALPERT, E