谷固醇血症
Sitosterolemia
定义 英文原文(暂无中文)
Sitosterolemia is a rare autosomal recessive sterol storage disease characterized by the accumulation of phytosterols in the blood and tissues. Clinical manifestations include xanthomas, arthralgia and premature atherosclerosis. Hematological manifestations include hemolytic anemia with stomatocytosis and macrothrombocytopenia. The disease is caused by homozygous or compound heterozygous mutations in ABCG5 (2p21) and ABCG8 (2p21) genes.
别名
植物固醇血症
基本事实
- 遗传方式
- 常染色体隐性
- 发病年龄
- 各年龄段
- 患病率
- <1 / 1 000 000
相关基因 2
| 基因 | 名称 | 关联类型 |
|---|---|---|
| ABCG5 | ATP binding cassette subfamily G member 5 | Disease-causing germline mutation(s) in |
| ABCG8 | ATP binding cassette subfamily G member 8 | Disease-causing germline mutation(s) in |
临床表型 13
常见 79–30%11
- 关节疼痛 HP:0002829
- 循环肝转氨酶水平升高 HP:0002910
- 循环谷固醇浓度增加 HP:0033341
- 巨血小板 HP:0001902
- 溶血性贫血 HP:0001878
- 高胆固醇血症 HP:0003124
- 巨血小板减少症 HP:0040185
- 早发性冠心病 HP:0005181
- 脾肿大 HP:0001744
- 口形红细胞增多症 HP:0004446
- 黄瘤病 HP:0000991
偶见 29–5%2
- 主动脉瓣狭窄 HP:0001650
- 关节痛/关节炎 HP:0005059
近两年的全球研究 178L2
2024/10 起在 Europe PMC 检索所得,按发表时间倒序显示最近 20 篇。标题未译成中文——自动翻译需要接入 LLM 服务,尚未引入。
- 2026-10Sitosterolemia presenting as unexplained cytopenias: hematologic manifestations and genetic spectrum
- 2026-09综述开放获取Familial Hypercholesterolemia
- 2026-09Hematologic manifestations of sitosterolemia: Phenotypic spectrum and long-term outcomes in seven genetically confirmed patients
- 2026-09综述Sitosterolemia: evolving strategies for earlier diagnosis
- 2026-09综述病例报告开放获取Phenotypic and Genotypic Landscape of Sitosterolemia in China: Including a Rare Case With Nephronophthisis
- 2026-09Sitosterolemia in pregnancy: A rare lipid disorder and its obstetric management
- 2026-08开放获取Increased LDL-C reduction with ezetimibe in ketogenic diet-induced hypercholesterolemia
- 2026-08开放获取Genetic Spectrum of Familial Hypercholesterolemia in Russian North-West Registry: Focus on Correlation Between Clinical and Genetic Diagnosis
- 2026-08Sitosterolemia as a treatable and underrecognized cause of chronic thrombocytopenia beyond ITP: A targeted screening study
- 2026-08Reverse Cascade Genetic Screening for Revealing New Cases of Familial Hypercholesterolemia in Russia: Pilot Project
- 2026-08开放获取When Lipid-Lowering Therapy Fails: Lessons From Functional Genomics and Precision Lipidology
- 2026-07Beyond sitosterol: A multivariable sterol model improves diagnosis of pediatric sitosterolemia in the gray zone
- 2026-07综述开放获取Decoding Primary Hyperlipoproteinemias: A Focus on the Pathogenesis and Diagnosis of Familial Hypercholesterolemia and Familial Combined Hyperlipidemia
- 2026-07综述开放获取Molecular genetic basis and clinical heterogeneity of sitosterolemia: focusing on the mutation spectrum and pathogenic mechanisms of ABCG5/ABCG8 genes
- 2026-07综述开放获取Adenosine triphosphate-binding cassette transporters: key players in maintaining fetal health during pregnancy
- 2026-07综述开放获取The Spectrum of Genetic Causes of Familial Hypercholesterolemia Phenotype
- 2026-07开放获取Cocrystals of β-Sitosterol with Propionic Acid Improve Postprandial Lipid Response and Long-Term Adaptation to Obesogenic Diets in Hamsters, Surpassing the Effects of Commercial β-Sitosterol
- 2026-07病例报告开放获取Homozygous familial hypercholesterolemia, experience with Evinacumab treatment in two Mexican pediatric patients: case report
- 2026-06综述开放获取From Phenotype to Genotype and Beyond: Insights into Familial Hypercholesterolemia and Familial Hypertriglyceridemia
- 2026-06综述开放获取Genetic Influence on LDL-Cholesterol Levels: Role of Polygenic Risk Scores and Lp(a) Beyond Monogenic Hypercholesterolemia
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)