Cargando…
Phenotyping of a novel COL4A4 and novel GLA variant in a patient presenting with microhematuria and mildly impaired kidney function: a case report
We describe the case of a 44-year-old male patient with a longstanding history of microhematuria and mildly impaired kidney function (CKD G2A1). The family history disclosed three females who also had microhematuria. Genetic testing by whole exome sequencing revealed two novel variants in COL4A4 (NM...
Autores principales: | Ponleitner, Markus, Allmer, Daniela Maria, Hecking, Manfred, Gatterer, Constantin, Graf, Senta, Smogavec, Mateja, Laccone, Franco, Rommer, Paulus Stefan, Sunder-Plassmann, Gere |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267447/ https://www.ncbi.nlm.nih.gov/pubmed/37323669 http://dx.doi.org/10.3389/fgene.2023.1211858 |
Ejemplares similares
-
A Single Lung Transplant in a Patient with Fabry Disease: Causality or Far-Fetched? A Case Report
por: Gaggl, Martina, et al.
Publicado: (2013) -
Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis
por: Frese, Jenny, et al.
Publicado: (2019) -
Long-Term Monitoring of Cardiac Involvement under Migalastat Treatment Using Magnetic Resonance Tomography in Fabry Disease
por: Gatterer, Constantin, et al.
Publicado: (2023) -
Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations
por: Rehder, Helga, et al.
Publicado: (2023) -
Prevalencia de microhematuria en población universitaria
por: Valdivieso Linares, Maricruz
Publicado: (2004)