Mevalonate Kinase Deficiency

Autosomal recessive disorder caused by mutations in the mevalonate kinase gene. Because of the mutations cholesterol biosynthesis is disrupted and MEVALONIC ACID accumulates. It is characterized by a range of symptoms, including dysmorphic FACIES, psychomotor retardation, CATARACT, hepatosplenomegaly, CEREBELLAR ATAXIA, elevated IMMUNOGLOBULIN D, and recurrent febrile crises with FEVER; LYMPHADENOPATHY; ARTHRALGIA; EDEMA; and rash.

Also Known As:

Hyper IgD Syndrome; Hyper-IgD Syndrome; Hyperimmunoglobulinemia D And Periodic Fever Syndrome; Mevalonic Aciduria; Periodic Fever, Dutch Type; Aciduria, Mevalonic; Hyper IgD Syndromes; Hyper-IgD Syndromes; Kinase Deficiencies, Mevalonate; Kinase Deficiency, Mevalonate; Mevalonate Kinase Deficiencies; Mevalonicacidurias; Syndrome, Hyper-IgD; Hyperimmunoglobulinemia D; Mevalonicaciduria

Nervous System Diseases: 14178
- Central Nervous System Diseases: 4213
  - Brain Diseases: 15694
    - Metabolic Brain Diseases: 215
      - Inborn Metabolic Brain Diseases: 2
        Mevalonate Kinase Deficiency: 310
Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Blood Protein Disorders: 17
    - Hypergammaglobulinemia: 1293
      - Mevalonate Kinase Deficiency: 310
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Peroxisomal Disorders: 504
      - Mevalonate Kinase Deficiency: 310
    - Inborn Metabolic Brain Diseases: 2
      - Mevalonate Kinase Deficiency: 310
  - Hereditary Autoinflammatory Diseases: 43
    - Mevalonate Kinase Deficiency: 310
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Peroxisomal Disorders: 504
      - Mevalonate Kinase Deficiency: 310
    - Inborn Metabolic Brain Diseases: 2
      - Mevalonate Kinase Deficiency: 310
  - Metabolic Brain Diseases: 215
    - Inborn Metabolic Brain Diseases: 2
      - Mevalonate Kinase Deficiency: 310
Immune System Diseases: 4321
- Immunoproliferative Disorders: 29
  - Hypergammaglobulinemia: 1293
    - Mevalonate Kinase Deficiency: 310

Sandra W M Buurman Selected Research

Sandra W M Buurman Research Topics

Disease

Drug/Important Bio-Agent (IBA)