par Squatrito, Sebastiano;Delange, François ;Trimarchi, Francesco;Lisi, Ermanna;Vigneri, Riccardo
Référence Journal of endocrinological investigation, 4, 3, page (295-302)
Publication Publié, 1981
Référence Journal of endocrinological investigation, 4, 3, page (295-302)
Publication Publié, 1981
Article révisé par les pairs
Résumé : | This work reports the presence of endemic cretinism in a small district located inside an endemic goiter area in north-eastern Sicily, personally described. The study covers 19 mental defectives (11 females and 8 males, mean age 35.8 ± 15.5 yr) selected on the basis of severe mental retardation recognized by the local doctors. No systematic survey for cretinism was carried out in the total population. Marked mental retardation was evident in all subjects. Nine of them exhibited clinical and biochemical signs of hypothyroidism (myxedematous cretins). The 10 others were clinically euthyroid and had deaf-mutism and/or pyramidal tract dysfunction (neurological cretinism). Familial aggregation of cretinism was also observed. In both myxedematous and neurological cretins the urinary iodine excretion was very low, but not significantly different from that recorded in the euthyroid controls of the same area. The data available do not clarify the pathogenesis of endemic cretinism in Sicily. However, the marked height retardation, the observation of delayed bone maturation and the severity of mental deficiency suggest that thyroid failure was present in early life. The presence of endemic cretinism today in Sicily constitutes a strong argument in favour of the immediate introduction of adequate iodine prophylaxis. © 1981, Italian Society of Endocrinology (SIE). All rights reserved. |