Meningococcemia
What's New
Last Posted: Feb 10, 2022
- Genetic workup as a complementary tool for the diagnosis of primary complement component deficiencies: a multicenter experience.
Shamriz Oded et al. European journal of pediatrics 2022 - MBL2 deficiency is associated with higher genomic bacterial loads during meningococcemia in young children.
Darton T C, et al. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 2014 12 (12) 1337-42 - Toll-like receptor 9 polymorphisms are associated with severity variables in a cohort of meningococcal meningitis survivors.
Sanders Marieke S, et al. BMC infectious diseases 2012 0 (1) 112 - Meningococcemia
From NCATS Genetic and Rare Diseases Information Center - 4G4G genotype of the plasminogen activator inhibitor-1 promoter polymorphism associates with disseminated intravascular coagulation in children with systemic meningococcemia.
Binder A, et al. Journal of thrombosis and haemostasis : JTH 2007 10 (10) 2049-54 - Protein C promoter polymorphisms associate with sepsis in children with systemic meningococcemia.
Binder Alexander, et al. Human genetics 2007 9 (2) 183-90 - Polymorphisms in the interleukin-1 gene cluster in children and young adults with systemic meningococcemia.
Endler Georg, et al. Clinical chemistry 2006 3 (3) 511-4 - Associations between Fc gamma receptor IIA polymorphisms and the risk and prognosis of meningococcal disease.
Domingo Pere, et al. The American journal of medicine 2002 1 (1) 19-25
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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