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克兰费尔特综合征伴发类似肯尼迪病的进行性肌肉萎缩。

Klinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's disease.

作者信息

Caballero Pedro Enrique Jiménez

机构信息

Department of Neurology, San Pedro de Alcántara Hospital, Avenida Pablo. Cáceres. Spain.

出版信息

Ann Indian Acad Neurol. 2012 Jul;15(3):227-9. doi: 10.4103/0972-2327.99730.

Abstract

Kennedy's disease, an X-linked spinal and bulbar muscular atrophy, is characterized by loss of lower motor neurons. Mild sensory deficits, gynecomastia and infertility may be observed. Klinefelter's syndrome is a variation of sex chromosome disorder characterized by hypogonadism, gynecomastia and azoospermia, and the most frequent karyotype is XXY. A 55-year-old man who presented with slowly progressive and diffuse neurogenic muscle atrophy without bulbar or sensory symptoms. He also had Klinefelter's syndrome. Genetic study of Kennedy's disease was normal. Our patient differs from those with Kennedy's disease in the absence of bulbar and sensory symptoms. It is suggested that the X chromosome plays an important role in the biology of motor neurons.

摘要

肯尼迪病是一种X连锁的脊髓和延髓肌肉萎缩症,其特征是下运动神经元丧失。可能会观察到轻度感觉缺陷、男性乳房发育和不育。克兰费尔特综合征是性染色体疾病的一种变体,其特征是性腺功能减退、男性乳房发育和无精子症,最常见的核型是XXY。一名55岁男性,表现为缓慢进展的弥漫性神经源性肌肉萎缩,无延髓或感觉症状。他还患有克兰费尔特综合征。肯尼迪病的基因研究结果正常。我们的患者与肯尼迪病患者不同,没有延髓和感觉症状。这表明X染色体在运动神经元生物学中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c5a/3424807/c922b02efcc9/AIAN-15-227-g001.jpg

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