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Noonan syndrome努南综合征

Noonan syndrome is a genetic disorder.努南综合征是一种遗传性疾病。 It affects between 1 in 1,000 to 1 in 2,500 people.它影响之间的一,在1000至1在2500人。 It can vary in severity, and mildly-affected individuals may remain undiagnosed.它可以在不同的严重性,和轻度影响的个人可能仍然undiagnosed 。 The disorder is characterised by a range of symptoms and physical features.无序的特点是由一系列症状及身体特征。 It is often associated with heart defects and short stature.它往往是与心脏缺陷和身材矮小。 Facial characteristics may appear to change as the individual ages.面部特征可能会出现改变,因为个人的千古罪人。

Noonan Syndrome takes its name from Dr. Jacqueline Noonan, a Paediatric Cardiologist in the United States.努南综合征需要它的名字从博士杰奎琳努南,儿科心脏病在美国。 She noticed that many children attending her clinic with narrowing of the pulmonary valves were also short and had similar facial features.她注意到,许多儿童参加她的诊所与缩小肺动脉瓣膜也短了类似的面部特征。 The first description was in 1963.首次描述是在1963年。