查询词典 phenylketonuria

At least half of patients with X-ALD are adults with somewhat milder manifestations, and women who are carriers may become symptomatic. X-ALD is often misdiagnosed as attention-deficit/hyperactivity disorder in boys and as multiple sclerosis in men and women, and is not an uncommon cause of Addison disease;(2) the incidence of X-ALD, estimated to be 1:17 000 in all ethnic groups, approximates that of phenylketonuria;(3) noninvasive and presymptomatic diagnosis and prenatal diagnosis are available; family screening and genetic counseling are key to disease prevention; and (4) new therapies, applied early, show promise.

至少1半的X-ALD为成年病人，表现较轻，而作为携带者的女性也可发病。X-ALD在男孩常误诊为注意缺陷/多动综合征，男女可误诊为多发性硬化，并且也是Addison病的病因；(2)据估计X-ALD发病率为1：17 000，类似于苯丙酮尿症；(3)可进行无创性、症状前诊断和产前诊断；家系筛查和遗传咨询是疾病预防的关键；(4)早期采用新的治疗方法非常具有前景。

At least half of patients with X-ALD are adults with somewhat milder manifestations, and women who are carriers may become symptomatic. X-ALD is often misdiagnosed as attention-deficit/hyperactiity disorder in boys and as multiple sclerosis in men and women, and is not an uncommon cause of Addison disease;(2) the incidence of X-ALD, estimated to be 1:17 000 in all ethnic groups, approximates that of phenylketonuria;(3) noninasie and presymptomatic diagnosis and prenatal diagnosis are aailable; family screening and genetic counseling are key to disease preention; and (4) new therapies, applied early, show promise.

至少1半的X-ALD为成年病人，表现较轻，而作为携带者的女性也可发病。X-ALD在男孩常误诊为注意缺陷/多动综合征，男女可误诊为多发性硬化，并且也是Addison病的病因；(2)据估计X-ALD发病率为1：17 000，类似于苯丙酮尿症；(3)可进行无创性、症状前诊断和产前诊断；家系筛查和遗传咨询是疾病预防的关键；(4)早期采用新的治疗方法非常具有前景。

For this reason, saccharin has been prohibited for decades in Canada, and the same is true for cyclamate in the USA, and aspartame is contraindicated in some people, such as those who suffer from phenylketonuria.

鉴于此原因，一些糖精产品分别在加拿大、美国被禁用几十年，或者对于一些人禁忌。

Medical food Phenylketonuria food, protein-free bars

医疗食物类抗苯丙酮酸尿症食物，无蛋白质棒

Objective To study the method for gene diagnosis of phenylketonuria.

目的 探讨苯丙酮尿症的基因诊断方法。

Objective To increase the success rate of prenatal diagnosis for classical phenylketonuria.

目的提高经典型苯丙酮尿症的产前诊断的成功率。

Objective To compare two methods of phenylketonuria screening for newborn.

目的 比较筛查新生儿苯丙酮尿症的2种检测苯丙氨酸的方法―细菌抑制法和荧光法。

He/she might also take a sample from baby s heel to test for phenylketonuria.

他/她也可能采取的样本，从婴儿s足跟，以测试为苯丙酮尿症。

And based on this principle,fluorescence detection system for neonatal phenylketonuria screening is designed.

如果在婴儿出生早期没有得到及时诊断和治疗，在发育过程中，高浓度的苯丙氨酸会严重损害婴儿的神经系统，将导致病儿不可逆的智力障碍，所以对其早期筛查尤为重要[1~3]。

Phenylketonuria is a genetic disease that is tested for at birth.

苯丙酮尿症是一种遗传疾病，在出生即测试。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。