一个罕见的Fanconi贫血相关核酶1突变病例报告,导致性综合征
Raja Sekar1, Ilakyaa Rajakumar1, Gerry G Mathew1
1Nephrology, SRM Medical College Hospital and Research Centre, Chengalpattu, IND.
Cureus
|August 8, 2024
概括
这一案例突出了罕见的Fanconi贫血相关核酶1 (FAN1) 突变,导致年轻人患脏疾病. 基因分析发现了FAN1突变,导致脏范围蛋白尿和慢性病 (CKD).
科学领域:
- 科和医学遗传学
- 研究影响功能的罕见遗传突变.
背景情况:
- 慢性病 (CKD) 通常具有复杂的病因,包括遗传因素.
- 芬科尼贫血相关核酶1 (FAN1) 基因突变很少与原发性病有关.
更多相关视频
12:47Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
38.4K
09:34Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
33.7K
相关概念视频
Nephrons
2.3K
The kidneys are intricate organs with millions of working units known as nephrons. Each nephron features two major structures: the renal corpuscle, which facilitates blood plasma filtration, and the renal tubule, which handles the glomerular filtrate. Blood supply is directly linked to the nephrons. The renal corpuscle consists of the glomerulus, a capillary network, and the Bowman's capsule, a double-walled epithelial structure that encases the glomerulus. The filtering of blood plasma...
2.3K
Nucleotide Excision Repair
37.0K
Overview
37.0K
Notch Signaling Pathway
4.2K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
4.2K
Cystic Fibrosis: Pathogenesis
201
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
201
Mutations
81.3K
Overview
81.3K
