DeLong G R, Stanbury J B, Fierro-Benitez R
Dev Med Child Neurol. 1985 Jun;27(3):317-24. doi: 10.1111/j.1469-8749.1985.tb04542.x.
Neurological examinations were made of 67 children and adults with congenital iodine-deficiency disorder (endemic cretinism) in four rural villages in highland Ecuador. There was a distinct and readily identifiable pattern of neurological deficits. These included, to varying degrees: deaf-mutism or lesser degrees of bilateral hearing-loss or dysarthria; spasticity, particularly involving the proximal lower extremities; mental deficiency of a characteristic type; and rigidity and bradykinesia. Not all of these elements were found in all cases. Less common features were strabismus, kyphoscoliosis and frontal-lobe signs. There were exceptional cases with hypotonia. In contrast, cerebellar function was largely spared, as were functions of emotion and attention, vegetative and autonomic functions, social interaction, and probably memory, except in the most severely involved.
对厄瓜多尔高地四个乡村的67名患有先天性碘缺乏症(地方性克汀病)的儿童和成人进行了神经学检查。存在一种明显且易于识别的神经功能缺损模式。这些缺损包括不同程度的:聋哑或较轻程度的双侧听力丧失或构音障碍;痉挛,尤其累及下肢近端;特定类型的智力缺陷;以及僵硬和运动迟缓。并非所有病例都出现了所有这些症状。不太常见的特征有斜视、脊柱侧弯和额叶体征。也有肌张力减退的罕见病例。相比之下,小脑功能基本未受影响,情感和注意力功能、植物神经和自主神经功能、社交互动以及可能的记忆功能也是如此,除了病情最严重的患者。