<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(6)</volume><submitter>Chumakova OS</submitter><pubmed_abstract>Inherited cardiomyopathies (CMPs) are fairly common causes of morbidity and mortality, particularly, in young individuals. In substantial number of cases, only morphological diagnostic criteria cannot distinguish one CMP from another because of incomplete penetrance, advanced stage of the disease, or overlapping phenotypes. Genetic testing has become a mandatory tool for definite diagnosis that is required for family screening, individual prognosis, and personalized treatment strategy in routine practice. In parallel, accumulation of genotype-phenotype correlations, especially for rare genes, promotes the deciphering of underling molecular mechanisms and the development of targeting treatment of CMPs. Here we present an adult-onset case comprised morphological features of several CMPs: asy</pubmed_abstract><journal>Cardiology research</journal><pagination>398-404</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9822668</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Overlapping Phenotype of Adult-Onset &lt;i>ALPK3&lt;/i>-Cardiomyopathy in the Setting of Two Novel Variants.</pubmed_title><pmcid>PMC9822668</pmcid><pubmed_authors>Zateyshchikov DA</pubmed_authors><pubmed_authors>Zakharova EY</pubmed_authors><pubmed_authors>Sinitsin VE</pubmed_authors><pubmed_authors>Milovanova NV</pubmed_authors><pubmed_authors>Bychkov IO</pubmed_authors><pubmed_authors>Mershina EA</pubmed_authors><pubmed_authors>Chumakova OS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Overlapping Phenotype of Adult-Onset &lt;i>ALPK3&lt;/i>-Cardiomyopathy in the Setting of Two Novel Variants.</name><description>Inherited cardiomyopathies (CMPs) are fairly common causes of morbidity and mortality, particularly, in young individuals. In substantial number of cases, only morphological diagnostic criteria cannot distinguish one CMP from another because of incomplete penetrance, advanced stage of the disease, or overlapping phenotypes. Genetic testing has become a mandatory tool for definite diagnosis that is required for family screening, individual prognosis, and personalized treatment strategy in routine practice. In parallel, accumulation of genotype-phenotype correlations, especially for rare genes, promotes the deciphering of underling molecular mechanisms and the development of targeting treatment of CMPs. Here we present an adult-onset case comprised morphological features of several CMPs: asy</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-07-14T22:15:55.049Z</modification><creation>2024-12-03T21:21:03.337Z</creation></dates><accession>S-EPMC9822668</accession><cross_references><pubmed>36660067</pubmed><doi>10.14740/cr1449</doi></cross_references></HashMap>