一种罕见可治疗的神经代谢障碍的症状性部震:一个病例报告
Ranadheer Jadala1, Umamaheswari Elumalai2, Arun Kumar Natesan3
1Resident, Department of Neurology, Madras Medical College, Chennai, Tamil Nadu, India.
The Journal of the Association of Physicians of India
|August 20, 2024
概括
palatal tremor (PT) 是 involuntary palate movement ( involuntary palate movement) 一种 involuntary palate movement (非自愿的 palatal movement) 的意思,它是一种罕见的脑肌质松症 (CTX) 的症状. 这项研究强调PT在CTX患者中是一个被诊断不足的症状,扩大了这种罕见的神经代谢疾病的已知的临床特征.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 口腔震 (PT) 涉及非自愿的,节奏的软口腔运动,被分类为基本的 (EPT) 或症状的 (SPT).
- 症状性PT是由吉兰-莫拉雷三角形中的病变引起的,而EPT没有确定的结构原因.
- 大脑肌性桑托马托症 (CTX) 是一种罕见的自体递归神经代谢疾病,具有多种神经和非神经表现.
研究的目的:
- 在患有大脑肌性桑托马托सिस (CTX) 的患者中报告两例 palatal tremor (PT) 病例.
- 强调PT作为一个潜在的诊断不足的临床征兆在CTX的扩张表型.
主要方法:
- 连续两名被诊断患有大脑肌性桑托马托斯 (CTX) 的患者的病例报告.
- 临床检查和评估神经和非神经特征,包括口腔震.
主要成果:
- 这两位患者都呈现了口腔震 (PT) 作为大脑状松病 (CTX) 的临床表现.
- 在这些案例中,PT的存在表明它是CTX中的一个相关的,尽管可能被忽视的标志.
结论:
- 口腔震 (PT) 可能是大脑肌质桑托马托सिस (CTX) 的出现或相关征兆.
- 这些发现提倡在CTX患者中提高PT的认识和诊断考虑,扩大对CTX临床谱的理解.
更多相关视频
相关概念视频
Inborn Errors of Metabolism
148
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
148
Disorders of the Skeletal Muscle
913
The clinical conditions affecting the skeletal muscle tissue are broadly categorized as musculoskeletal and neuromuscular disorders.
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
913
Parkinson's Disease: Treatment
240
Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...
240
Myasthenia Gravis: Overview and Treatment
1.3K
Myasthenia gravis is a neuromuscular transmission disorder characterized by weakness and increased fatigability of skeletal muscles. It is an autoimmune disease affecting approximately one in 2000 people, where antibodies against the α1 subunit of nicotinic acetylcholine receptors are produced.
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
1.3K
Parkinson's Disease: Overview
501
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...
501
Myasthenia Gravis: Diagnostic Tests
714
Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
714


