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先天性鱼鳞病综合征、神经感觉性耳聋、智力发育迟缓、牙发育不全、短指(趾)畸形、小指(趾)内翻、副颈肋和甲状腺癌。

Syndrome of ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and carcinoma of the thyroid.

作者信息

Ruzicka T, Goerz G, Anton-Lamprecht I

出版信息

Dermatologica. 1981;162(2):124-36. doi: 10.1159/000250259.

Abstract

We report the case of a 15-year-old girl with a uneventful family history. Her skin condition was clinically, histologically and ultrastructurally compatible with the diagnosis of ichthyosis congenita. She suffered from neurosensory deafness and oligophrenia. Further findings included dental aplasia, brachydactyly, clinodactyly and accessory cervical ribs. At the age of 14, a thyroid carcinoma was diagnosed. Therapy with a retinoid derivative (Ro 10-9359) resulted in a marked improvement of the ichthyosis. We assume a genetic syndrome with autosomal-recessive inheritance.

摘要

我们报告了一名15岁女孩的病例,其家族史无异常。她的皮肤状况在临床、组织学和超微结构上与先天性鱼鳞病的诊断相符。她患有神经感觉性耳聋和智力发育迟缓。进一步的检查结果包括牙齿发育不全、短指畸形、小指内翻和副颈肋。14岁时,她被诊断出患有甲状腺癌。使用维甲酸衍生物(Ro 10-9359)治疗后,鱼鳞病有明显改善。我们推测这是一种常染色体隐性遗传的基因综合征。

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