Mesangial Proliferative Glomerulonephritis
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Last Posted: Sep 07, 2023
- [Genetic analysis of a patient with Alport syndrome due to compound heterozygous variants of COL4A4 gene].
Bingbing Yang, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 0 (9) 1150-1154 - Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
Deng Haiyue, et al. Molecular genetics & genomic medicine 2020 0 (8) e1306 - Novel pathogenic OCRL mutations and genotype-phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review.
Zhang Yu, et al. BMC medical genomics 2021 0 (1) 219 - Angiotensin-converting enzyme genotype is not a significant genetic risk factor for idiopathic nephrotic syndrome in Croatian children.
Batini? Danko, et al. Nephron 2015 0 (1) 29-34 - Association of human leukocyte antigen gene polymorphism and mesangial proliferative glomerulonephritis in a large population-based study.
Zhao Jing-Jie, et al. Biomedical reports 2013 9 (5) 751-756 - Complement factor H gene associations with end-stage kidney disease in African Americans.
Bonomo Jason A, et al. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 7 (7) 1409-14 - Impact of the -675 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene on childhood IgA nephropathy.
Han Su-Ryun, et al. Experimental and therapeutic medicine 2012 4 (4) 703-706 - Mesangial proliferative glomerulonephritis
From NCATS Genetic and Rare Diseases Information Center - The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.
Reiterová J, et al. Folia biologica 2007 0 (4) 134-7 - Interleukin-6 gene polymorphism and faster progression to end-stage renal failure in chronic glomerulonephritis.
Buraczynska Monika, et al. Translational research : the journal of laboratory and clinical medicine 2007 8 (2) 101-5
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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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