Mucolipidosis IV.

F Goutières, M L Arsenio-Nunes, J Aicardi
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Abstract

Five new cases of Mucolipidosis IV are related and the seven cases in the literature reviewed. Neurological signs of the disorder and the value of skin and conjuncitival biopsies for its diagnosis are emphasized. Arguments in favour of a recessive autosomic inheritance are brought forth. The disease does not affect exclusively Jewish people. In two cases absence of oligosacchariduria was demonstrated.

粘脂病IV。
本文报道5例新发黏液脂质沉积症,并对文献报道的7例进行综述。神经症状的障碍和价值的皮肤和结膜活检的诊断强调。提出了赞成隐性常染色体遗传的论点。这种疾病并不只影响犹太人。2例无低糖尿。
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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