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与RNA聚合酶III相关的脑白质营养不良中的神经源性膀胱和神经内分泌异常。

Neurogenic bladder and neuroendocrine abnormalities in Pol III-related leukodystrophy.

作者信息

Potic Ana, Popovic Vera, Ostojic Jelena, Pekic Sandra, Kozic Dusko, Guerrero Kether, Schiffmann Raphael, Bernard Geneviève

出版信息

BMC Neurol. 2015 Mar 4;15:22. doi: 10.1186/s12883-015-0283-7.

Abstract

BACKGROUND

Pol III-related leukodystrophies, including 4H leukodystrophy, are recently recognized disorders that comprise hypomyelination and various neurologic and non-neurologic clinical manifestations. We report the unique neurologic presentation of the micturition dysfunction in Pol III-related leukodystrophy and describe the novel endocrine abnormalities in this entity.

CASE PRESENTATION

A 32-year-old Caucasian female exhibited chronic urinary incontinence that commenced at the age of 7 years and remained the unexplained symptom more than two decades before the onset of progressive neurologic decline. A transient growth failure and absent sexual development with hypoprolactinemia appeared in the meanwhile. Neurologic, endocrine, neuroradiologic, and genetic evaluation performed only in the patient's thirties, confirmed the diagnosis of 4H leukodystrophy as the only cause of the micturition disturbance.

CONCLUSION

The report shows for the first time that an unexplained chronic bladder dysfunction should be evaluated also as a possible 4H leukodystrophy, thus alerting to the unexpected neurologic and endocrine features in 4H leukodystrophy.

摘要

背景

包括4H型脑白质营养不良在内的与RNA聚合酶III相关的脑白质营养不良是最近才被认识的疾病,其特征包括髓鞘形成不足以及各种神经和非神经临床表现。我们报告了与RNA聚合酶III相关的脑白质营养不良中排尿功能障碍的独特神经学表现,并描述了该疾病新出现的内分泌异常。

病例介绍

一名32岁的白种女性自7岁起出现慢性尿失禁,在进行性神经功能衰退开始前的二十多年里,这一症状一直无法解释。与此同时,出现了短暂的生长发育迟缓以及伴有低催乳素血症的性发育停滞。仅在患者三十多岁时进行的神经学、内分泌学、神经放射学和遗传学评估,确诊4H型脑白质营养不良是排尿障碍的唯一病因。

结论

该报告首次表明,不明原因的慢性膀胱功能障碍也应作为4H型脑白质营养不良的一种可能情况进行评估,从而提醒人们注意4H型脑白质营养不良中意想不到的神经学和内分泌特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ac/4351912/4c0d1f05118b/12883_2015_283_Fig1_HTML.jpg

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