<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>158(9)</volume><submitter>Trefzer L</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>Kidney-urinary tract (KUT) manifestations cause substantial morbidity in patients with junctional epidermolysis bullosa (JEB), but the spectrum of disease severity and the clinical course have been poorly characterized.&lt;h4>Objective&lt;/h4>To examine in a large cohort of patients with intermediate JEB the KUT manifestations, diagnostic and therapeutic procedures, genotype-phenotype correlations, and outcomes as a basis for recommendations, prognosis, and management.&lt;h4>Design, setting, and participants&lt;/h4>In this retrospective, longitudinal case series study, 99 patients with a diagnosis of JEB based on clinical and genetic findings who were treated in a single dermatology department in Freiburg, Germany, were assessed during an 18-year period (January 1, 2003, to December</pubmed_abstract><journal>JAMA dermatology</journal><pagination>1057-1062</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9350844</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Kidney-Urinary Tract Involvement in Intermediate Junctional Epidermolysis Bullosa.</pubmed_title><pmcid>PMC9350844</pmcid><pubmed_authors>Trefzer L</pubmed_authors><pubmed_authors>Pohl M</pubmed_authors><pubmed_authors>Nystrom A</pubmed_authors><pubmed_authors>Miernik A</pubmed_authors><pubmed_authors>Has C</pubmed_authors><pubmed_authors>Schwieger-Briel A</pubmed_authors><pubmed_authors>Conradt G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Kidney-Urinary Tract Involvement in Intermediate Junctional Epidermolysis Bullosa.</name><description>&lt;h4>Importance&lt;/h4>Kidney-urinary tract (KUT) manifestations cause substantial morbidity in patients with junctional epidermolysis bullosa (JEB), but the spectrum of disease severity and the clinical course have been poorly characterized.&lt;h4>Objective&lt;/h4>To examine in a large cohort of patients with intermediate JEB the KUT manifestations, diagnostic and therapeutic procedures, genotype-phenotype correlations, and outcomes as a basis for recommendations, prognosis, and management.&lt;h4>Design, setting, and participants&lt;/h4>In this retrospective, longitudinal case series study, 99 patients with a diagnosis of JEB based on clinical and genetic findings who were treated in a single dermatology department in Freiburg, Germany, were assessed during an 18-year period (January 1, 2003, to December</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-05-09T14:02:12.958Z</modification><creation>2025-04-07T04:16:14.644Z</creation></dates><accession>S-EPMC9350844</accession><cross_references><pubmed>35921091</pubmed><doi>10.1001/jamadermatol.2022.2885</doi></cross_references></HashMap>