Sankar R, Pulger T, Rai B, Sankar G, Gyatso T R, Rai B M
RIA laboratory, Govt. Gen. Hospital Namchi, S. Sikkim.
J Assoc Physicians India. 1993 Jun;41(6):337-8.
One hundred individuals suffering from Endemic Cretinism were studied. There were 55 males and 45 females. 62% of the cretins had visible goitre. Thirty nine (62.9%) goitrous cretins had grade II goitre. Neurological cretinism was the predominant type encountered (99%) and Myxoedematous cretinism was seen in only one patient. The most salient neurological feature was deaf-mutism seen in 74%. Findings in the motor system were, apart from deaf-mutism, the most characteristic feature of the condition on clinical examination. 58% had exaggerated deep tendon reflexes and 31% had extensor plantar response. Squint was noticed in 29%. Familial aggregation was noticed and was striking. Endemic cretinism is a distinctive and easily identifiable clinical entity and is an important indicator of the severity of iodine deficiency in a community.
对100例地方性克汀病患者进行了研究。其中男性55例,女性45例。62%的克汀病患者有可见的甲状腺肿。39例(62.9%)甲状腺肿性克汀病患者为Ⅱ度甲状腺肿。神经型克汀病是最常见的类型(99%),黏液水肿型克汀病仅见于1例患者。最突出的神经学特征是74%的患者出现聋哑。运动系统的表现,除聋哑外,是临床检查中该病最具特征性的表现。58%的患者深腱反射亢进,31%的患者有跖伸反应。29%的患者有斜视。发现有家族聚集现象,且很明显。地方性克汀病是一种独特且易于识别的临床实体,是社区碘缺乏严重程度的重要指标。