李氏状综合征与由新型HIBCH变体引起的渐进性小脑缩
Yoshihiro Taura1, Takenori Tozawa2,3, Kenichi Isoda4
1Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Human genome variation
|August 21, 2023
概括
在HIBCH基因的致病变体导致HIBCH缺陷,一个线粒体疾病影响代谢. 这种病例扩大了已知的症状,包括在李氏状综合征中的渐进性小脑缩.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 神经学 神经学
背景情况:
- HIBCH缺乏症是一种罕见的遗传性疾病,影响氨酸代谢,导致线粒体功能障碍.
- 临床表现通常包括发育问题,脑病变,低血压和 dystonia,在MRI上具有特征的基底腺病变.
研究的目的:
- 报告一个日本病人的HIBCH缺陷呈现为李氏状综合征的新型病例.
- 记录HIBCH缺乏症的扩大表型谱,包括渐进性小脑缩.
主要方法:
- 一位患有李氏状综合征的日本患者的临床病例报告.
- 基因分析以确定HIBCH基因中的致病变体.
- 纵向大脑磁共振成像 (MRI) 后续检查.
主要成果:
- 在患者中识别新的致病性HIBCH变体.
- 临床表现与李氏状综合征一致.
- 长期的MRI显示了渐进的小脑缩,这是以前没有报道的发现.
结论:
- 新的HIBCH变种可能会导致李氏状综合征.
- 渐进性小脑缩是HIBCH缺乏症的表型谱中新发现的一种特征.
- 这一发现扩大了对HIBCH相关线粒体疾病的理解.
相关概念视频
Parkinson's Disease: Overview
596
Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is...
596
Amyloid Fibrils
9.6K
Amyloid fibrils are aggregates of misfolded proteins. Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils.
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
9.6K
Lysosomal Hydrolases
3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K
Cardiomyopathy III: Hypertrophic Cardiomyopathy
16
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
16
Alzheimer's Disease: Overview
518
Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
518
Neural Regulation
39.5K
Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
39.5K


