[Languaje and hearing in Prader-Willi syndrome].

E Sánchez Legaza, M Ciges Juan, M González Pérez, J I Miranda Caravallo
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Abstract

Prader-Willi syndrome was described for the first time in 1956. Due to its lack of biological markers its diagnosis is a clinical one, taking into consideration that it varies with age. It is characterised by neonatal hypotonia, obesity, mild mental retardation or learning incapacity, behavioural problems, mainly towards food. Most aspects studied have been centred in medical and genetic aspects, whereas those related to hearing and language have been somewhat limited. We carry out a revision of those aspects.

[普瑞德-威利综合征的语言和听力]。
普拉德-威利综合征于1956年首次被描述。由于缺乏生物学标志物,它的诊断是临床的,考虑到它随年龄而变化。它的特点是新生儿张力不足,肥胖,轻度智力迟钝或学习能力低下,行为问题,主要是对食物。研究的大多数方面集中在医学和遗传方面,而与听力和语言有关的方面则有些有限。我们对这些方面进行了修订。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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