Progressive demyelinating childhood cerebral adrenoleukodystrophy : Assessment of communication impairment

Rare Pub Date : 2024-01-01 DOI:10.1016/j.rare.2024.100029
Mangal Chandra Yadav , Bhavani Venkatachalam , Akshay Parmar , M. Aparna Krishnan , Reheema Thasli , Sachchidanand Sinha
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Abstract

Adrenoleukodystrophy (ALD) is a rare demyelinating genetic disorder occurring due to mutation in the gene ABCD1. The current case study involved detailed evaluation of communication skills including audiological and speech-language evaluations of a 6 year old diagnosed with ALD. The child evidenced severely restricted communication skills along with several other subsystems affected.

进行性脱髓鞘儿童脑腺样体营养不良症:交流障碍评估
肾上腺白质营养不良症(ALD)是一种罕见的脱髓鞘遗传性疾病,由基因 ABCD1 突变引起。本病例研究涉及对一名被诊断为 ALD 的 6 岁儿童进行详细的沟通能力评估,包括听力和语言评估。该患儿的交流能力严重受限,其他几个子系统也受到影响。
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