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不伴同型半胱氨酸尿症的甲基丙二酸血症

Methylmalonic acidemia without homocystinuria

ORPHA:293355疾病组中国目录 第1批 · 71

定义

甲基丙二酸血症是一种先天性维生素B12代谢异常,其特征是由于线粒体酶甲基丙二酰辅酶A变位酶功能下降引起的胃肠道和神经代谢表现。

别名

甲基丙二酸尿症不伴高胱氨酸尿症

基本事实

遗传方式
常染色体显性、常染色体隐性、X 连锁显性
发病年龄
各年龄段
患病率
1-9 / 100 000(Europe)

近两年的全球研究 43L2

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。

  • 2026-09综述开放获取
    Precision Medicine in Pediatric Nephrology: From Shared Clinical Phenotypes to Genotype-Guided Diagnosis and Management
    Genes · DOI · Europe PMC
  • 2026-09病例报告开放获取
    Classical Homocystinuria Incidentally Diagnosed Following a Normal Newborn Screening Result
    International journal of neonatal screening · DOI · Europe PMC
  • 2026-09开放获取
    Adherence to Long-Acting Injectable Risperidone ISM in a Community Psychiatric Setting: A Real-World Observational Study
    European psychiatry : the journal of the Association of European Psych
  • 2026-09开放获取
    Neuropsychiatric Manifestations in Methylmalonic Acidemia and Homocystinuria of Adult Presentation. A Case Report
    European psychiatry : the journal of the Association of European Psych
  • 2026-08开放获取
    Cobalamin C Deficiency Presenting with CVID-like Immunologic Abnormalities: A Five-Patient Pediatric Case Series
    Journal of clinical immunology · DOI · Europe PMC
  • 2026-08开放获取
    The Spanish Uniform Newborn Screening Panel (SUSP): A National Consensus Framework for Harmonized Newborn Screening
    International journal of neonatal screening · DOI · Europe PMC
  • 2026-08
    Comparison of Medium-Coverage Whole-Genome Sequencing and Chromosomal Microarray in Prenatal Testing of Absence of Heterozygosity
    Prenatal diagnosis · DOI · Europe PMC
  • 2026-07开放获取
    Assessment of blood cobalt levels and safety of long-term hydroxocobalamin therapy in patients with cblC defect
    Frontiers in nutrition · DOI · Europe PMC
  • 2026-07综述开放获取
    Diagnosis and treatment of vitamin B12 deficiency in children
    Frontiers in nutrition · DOI · Europe PMC
  • 2026-05综述病例报告开放获取
    A child with cobalamin C deficiency caused by complex heterozygous variation of c.567dupT and c.80A > G complicated with pulmonary arterial hypertension and hydrocephalus: A case report and literature review
    Medicine · DOI · Europe PMC
  • 2026-04开放获取
    Sublingual methylcobalamin treatment in infants with prolonged jaundice due to vitamin B12 deficiency
    Frontiers in pediatrics · DOI · Europe PMC
  • 2026-04综述开放获取
    Carrier screening in the reproductive setting-Are there medical implications for the heterozygote?-A guide for clinicians
    Pregnancy (Hoboken, N.J.) · DOI · Europe PMC
  • 2026-03病例报告开放获取
    Encephalitis-like presentation of methylmalonic acidemia with homocystinuria in a postpartum woman: a case report
    Frontiers in psychiatry · DOI · Europe PMC
  • 2026-01病例报告开放获取
    Case Report: Dilated cardiomyopathy as the initial presentation in an adult with late-onset CblC defect
    Frontiers in cardiovascular medicine · 被引 1 · DOI · Europe PMC
  • 2025-12开放获取
    Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variation
    Journal of translational medicine · DOI · Europe PMC
  • 2025-12
    Underrecognized need for early detection of inborn errors of metabolism in China: A population-based study of 14.31 million residents (2012-2023)
    Molecular genetics and metabolism · DOI · Europe PMC
  • 2025-10病例报告开放获取
    Case Report: Cerebellar microhemorrhages: an underrecognized feature of MMA-HC revealed by high-field 7.0 T MRI
    Frontiers in radiology · DOI · Europe PMC
  • 2025-09综述
    The SLC-ome of membrane transport: From molecular discovery to physiology and clinical applications
    Physiological reviews · 被引 4 · DOI · Europe PMC
  • 2025-09开放获取
    Milder Form of Cobalamin C Disease May Be Missed by Newborn Screening: The Importance of Methylmalonic Acid Assessment
    International journal of neonatal screening · DOI · Europe PMC
  • 2025-08开放获取
    Analysis of hydroxocobalamin dosage in patients with CblC deficiency
    Orphanet journal of rare diseases · 被引 2 · DOI · Europe PMC

境外已获批用于本病的药物 0L2

欧盟与美国均未检索到已获批用于本病的药物。

尚未获批的在研药物(1 项)

这些药已被欧盟或美国的监管机构认定为罕见病用药(英文 orphan drug designation,中文行业里通称「孤儿药资格」——「孤儿」说的是这类药市场太小、没有厂商愿意认领,不是在说病人)。但这只是一种监管身份:意味着监管机构给予研发上的激励,不代表这个药已被证明有效,也不代表将来一定能上市,绝大多数最终不会成药。列在这里是为了看清有哪些方向正在被尝试。

  • messanger ribonucleic acid (mRNA)-based therapeutic agent encoding hum美国2018-03-07
    Treatment of isolated methylmalonic academia (MMA) due to methylmalonyl-Coenzyme A mutase (MUT) deficiency
    官方记录

数据来自欧洲药品管理局(EMA)的药品与罕见病用药资格公开导出表,以及美国 FDA 的罕见病用药资格数据库(Orphan Drug Product Designation Database)。两边口径不同:欧盟一侧取的是当前状态仍为「已授权」的药品;美国一侧记录的是「曾获批准」这一事实,FDA 的公开表不追踪药物此后是否退市(例如 Relyvrio 于 2024 年撤市,表中仍记为已获批)。请以官方记录页为准。

中国境外的在招试验 1L2

这些试验在中国没有研究中心,通常无法直接报名——入组一般要求在当地居住并接受随访。列在这里是因为它另有用处:看清楚全世界正在试哪些药、做到了哪一期、由谁在做。把药名和 NCT 编号记下来去问主治医生,或据此进一步查该药是否已在境外获批、是否有拓展性用药(expanded access)通道。

意大利1

共 2 项。

  • 尚未开始招募NCT07163364
    A Study to Evaluate the Effects and Safety of Hydroxocobalamin in Participants With Combined Methylmalonic Academia (cblC Type)
    III 期 · 干预性 · 2025/08/31CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
  • 招募中NCT04880356
    Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.
    观察性 · 2021/03/01Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
    意大利

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)