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首页> 外文期刊>Italian journal of pediatrics >Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report
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Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

机译:Prader-Willi综合征因异位舌下甲状腺引起的先天性甲状腺功能减退症:一例报告

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Background Thyroid gland disorders are variably associated with Prader-Willi syndrome (PWS). Many of the clinical features in newborns with PWS are similar to those found in congenital hypothyroidism (CH). Case presentation We report a case of a girl with CH and PWS. At the age of 9?months CH caused by an ectopic sublingual thyroid was diagnosed, and hormone replacement therapy was started. In spite of this treatment a decrease in growth velocity, weight excess and delayed development were observed. At the age of 9?years PWS was suspected on the basis of phenotype and genetic tests confirmed a maternal uniparental disomy of chromosome 15. This is the second reported case of hypothyroidism due to an ectopic sublingual thyroid gland in PWS suggesting that, although rare, an association between CH and PWS may exist. In our case diagnosis of PWS was delayed because mental retardation, hypotonia, obesity and short stature were initially attributed to hypothyroidism. Conclusions In this context PWS should be considered in obese children with CH who do not improve adequately with l-thyroxine therapy. Also, thyroid function in all PWS children should be assessed regularly in order to avoid delayed diagnosis of hypothyroidism.
机译:背景甲状腺疾病与Prader-Willi综合征(PWS)有不同的关联。患有PWS的新生儿的许多临床特征与先天性甲状腺功能减退症(CH)中发现的特征相似。病例介绍我们报告了一名患有CH和PWS的女孩的病例。在9个月大时,诊断出由异位舌下甲状腺引起的CH,并开始了激素替代治疗。尽管进行了这种处理,但观察到生长速度下降,体重增加和发育延迟。根据表型,怀疑PWS年龄为9岁,遗传学检查证实是母亲的15号单亲二体性二倍体。这是第二例甲状腺功能减退的报道病例,原因是PWS中存在异位的舌下甲状腺,这表明尽管罕见, CH和PWS之间可能存在关联。在我们的病例中,PWS的诊断被延迟,因为智力低下,肌张力低下,肥胖和身材矮小最初归因于甲状腺功能低下。结论在这种情况下,对于l-甲状腺素治疗不能充分改善的肥胖CH儿童应考虑PWS。此外,应定期评估所有PWS儿童的甲状腺功能,以免延误诊断甲状腺功能减退症。

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