Congenital pseudarthrosis of the leg bones and autistic spectrum disorder in a patient with neurofibromatosis type 1

R. Gamirova, K. R. Zabirova, A. R. Safina, E. A. Gorobets, S. Y. Volgina
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Abstract

The article presents an analysis of the pathogenesis of neurofibromatosis type 1, the mechanism of damage to the central nervous system. It analyzes the general clinical symptoms of neurofibromatosis type 1, its diagnostic criteria, describes the specifics of cognitive development in this disease with an emphasis on behavioral and autism spectrum disorders. The authors describe a clinical case of neurofibromatosis type 1 (a boy, 6 years and 10 months), in which, along with coffee-colored skin spots, subcutaneous fibromas, one of the first symptoms of the disease was also a congenital false joint of the bones of the left leg. Absence of speech development and autism spectrum disorders are key problems in the cognitive status of the child.
一名 1 型神经纤维瘤病患者的先天性腿骨假关节和自闭症谱系障碍
文章分析了神经纤维瘤病 1 型的发病机制、中枢神经系统的损伤机制。文章分析了 1 型神经纤维瘤病的一般临床症状、诊断标准,描述了该病认知发育的具体情况,重点是行为障碍和自闭症谱系障碍。作者描述了一个 1 型神经纤维瘤病的临床病例(男孩,6 岁 10 个月),病例中除了咖啡色的皮肤斑点和皮下纤维瘤外,该病的首发症状之一还包括左腿骨骼的先天性假关节。缺乏语言发育和自闭症谱系障碍是患儿认知状况的关键问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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