×
About 645 results

ALLMedicine™ Alport Syndrome Center

Research & Reviews  250 results

The Spectrum of Internal Limiting Membrane Disease in Alport Syndrome: a Multimodal Ima...
https://doi.org/10.1097/IAE.0000000000003295
Retina (Philadelphia, Pa.); Cicinelli MV, Ritter M et. al.

Sep 7th, 2021 - To characterize the spectrum of internal limiting membrane (ILM) disease in Alport syndrome (AS) using multimodal imaging, including widefield (WF) and ultra-widefield (UWF) modalities, and to report their relative prevalence according to the gene...

Prevalence Estimates of Predicted Pathogenic COL4A3-COL4A5 Variants in a Population Seq...
https://doi.org/10.1681/ASN.2020071065
Journal of the American Society of Nephrology : JASN; Gibson J, Fieldhouse R et. al.

Aug 18th, 2021 - The reported prevalence of Alport syndrome varies from one in 5000 to one in 53,000 individuals. This study estimated the frequencies of predicted pathogenic COL4A3-COL4A5 variants in sequencing databases of populations without known kidney diseas...

Role of multimodal ocular imaging in Alport syndrome.
https://doi.org/10.1016/j.jcjo.2021.06.018
Canadian Journal of Ophthalmology. Journal Canadien D'oph... Kapoor A, Kapoor S et. al.

Jul 30th, 2021 - Role of multimodal ocular imaging in Alport syndrome.|2021|Kapoor A,Kapoor S,Chawla R,|

Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3-COL4A5) and Their ...
https://doi.org/10.1053/j.ajkd.2021.04.017
American Journal of Kidney Diseases : the Official Journa... Savige J, Harraka P

Jul 11th, 2021 - Massively Parallel Sequencing identifies pathogenic variants in the genes affected in Alport syndrome (COL4A3 - COL4A5) in up to 30 % of individuals with focal and segmental glomerulosclerosis (FSGS), 10 % of those with kidney failure of unknown c...

Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family hist...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265006
European Journal of Medical Research; Ding Y, Tang X et. al.

Jul 10th, 2021 - Alport syndrome and C3 glomerulonephritis (C3GN) are rare kidney diseases, frequently responsible for familial haematuria, proteinuria, and renal impairment. With the rapid development of molecular genetic testing, Alport syndrome causes have been...

see more →

Guidelines  1 results

Clinical practice recommendations for the treatment of Alport syndrome: a statement of ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505543
Pediatric Nephrology (Berlin, Germany); Kashtan CE, Ding J et. al.

Mar 31st, 2012 - We present clinical practice recommendations for the treatment of children with Alport syndrome who are not enrolled in clinical trials. Our goal is to promote early initiation of a standard therapeutic approach that will facilitate assessment of ...

see more →

News  7 results

Alport Syndrome Research Funding Is Awarded
https://www.mdedge.com/pediatrics/article/148143/rare-diseases/alport-syndrome-research-funding-awarded

Sep 27th, 2017 - Researchers at the University of Miami in Florida and University of Cyprus have each been awarded $100,000 to explore two drug repurposing projects to identify possible treatments for Alport syndrome. The funding was provided by the Alport Syndrom.

External Resources and Information Related to Patients’ Experience
http://www.fda.gov/drugs/development-approval-process-drugs/external-resources-and-information-related-patients-experience

  This webpage is intended to facilitate public discussion of patient-focused drug development and evaluation. This webpage provides links to certain publicly available external reports and resources relating to patient experience data. The patien...

External Resources or Information Related to Patients’ Experience
http://www.fda.gov/drugs/development-approval-process-drugs/external-resources-or-information-related-patients-experience

This webpage is intended to facilitate public discussion of patient-focused drug development and evaluation. This webpage provides links to certain publicly available external reports and resources relating to patient experience data. The patient ...

Alport Syndrome Foundation Announces Research Funding
https://www.mdedge.com/clinicianreviews/article/131705/rare-diseases/alport-syndrome-foundation-announces-research-funding

Feb 17th, 2017 - The Alport Syndrome Foundation has announced the availability of funding for research to find novel treatments to prevent kidney failure and hearing loss in all patients with Alport syndrome. Two $100,000 projects are anticipated.

Funding Announced for Alport Syndrome Research
https://www.mdedge.com/familymedicine/article/111833/rare-diseases/funding-announced-alport-syndrome-research
The Journal of Family Practice;

Aug 15th, 2016 - The Alport Syndrome Foundation (ASF), Pedersen Family, and The Kidney Foundation of Canada (KFOC) Research Funding Program have announced that joint funding has been awarded for two new research projects on Alport syndrome, a rare genetic kidney d.

see more →