晚期发生的甲基马龙酸血症和同胞蛋白血症 (cblC病):系统性审查
Loredana Arhip1,2, Noemi Brox-Torrecilla3, Inmaculada Romero4
1Unidad de Nutrición Clínica y Dietética, Hospital General Universitario Gregorio Marañón, Calle del Doctor Esquerdo 46, 28007, Madrid, Spain. loredanarhip@gmail.com.
Orphanet journal of rare diseases
|January 20, 2024
概括
晚发性cblC疾病是一种常见的可巴胺代谢障碍,呈现出各种神经和系统症状. 早期治疗可以导致改善或康复,但对于不明确的病例,警至关重要.
科学领域:
- 生物化学 生物化学
- 遗传学 遗传学 是一个
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 结合甲基马龙酸血症和同胞素尿,cblC类型 (cblC疾病) 是细胞内可巴胺代谢最常见的遗传性疾病.
- 发病范围从产前到成年人,其特点是甲基马龙酸 (MMA) 和同类氨酸的升高,甲氨酸的产量减少.
研究的目的:
- 系统地审查晚发性cblC疾病的临床表现,诊断方法和结果.
- 巩固现有科学文献中关于这个特定患者队列的发现.
主要方法:
- 在PubMed (MEDLINE) 和参考列表中进行了全面的文献搜索.
- 搜索术语集中在cblC疾病和晚发病呈现上.
- 研究选择,数据提取和质量评估由两位独立审查员进行.
主要成果:
- 该综述包括来自65篇文章的199名患者,详细说明了神经病变,脑病变,精神问题,血栓性微血管病变,发作,脏疾病和肺高血压等常见症状.
- 使用了包括补充剂在内的各种治疗策略,有时是连续或并发的.
- 结果表明64名患者恢复,78名患者改善,4名患者没有改善或进展,12名患者死亡.
结论:
- 晚期发病的cblC文献主要包括病例报告和系列.
- 治疗的开始往往导致患者的改善或康复.
- 不完全康复突出了需要提高对cblC在模两可的临床表现的认识.
更多相关视频
03:19Author Spotlight: Studying the Impact of Maternal Dietary Deficiencies on Long-Term Offspring Health Outcomes
Published on: June 28, 2024
438
13:21Comprehensive DNA Methylation Analysis Using a Methyl-CpG-binding Domain Capture-based Method in Chronic Lymphocytic Leukemia Patients
Published on: June 16, 2017
10.0K
相关概念视频
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
Inborn Errors of Metabolism
160
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...
160
Smooth Endoplasmic Reticulum
5.8K
Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
5.8K
