<HashMap><database>biostudies-literature</database><scores/><additional><submitter>She D</submitter><funding>National Natural Science Foundation of China</funding><pagination>152</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7060591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare genetic disorder characterized by extraskeletal heterotopic ossification. It is well recognized that FOP can lead to a devastating condition of disability. However, the mortality rate of FOP patients in China and risk factors for mortality are still largely unclear.&lt;h4>Methods&lt;/h4>We conducted a retrospective research on a cohort of 65 cases of FOP patients in China from 2008 to 2018. We reviewed medical records of these FOP patients to retrieve information such as date of birth/death, gender, clinical features, genotypes and biochemical parameters and analyze the correlation of these parameters with the mortality.&lt;h4>Results&lt;/h4>92.3% (60/65 cases) patients were classic FOP patients, 3.1% (2/65 cases) were FOP</pubmed_abstract><journal>BMC musculoskeletal disorders</journal><pubmed_title>Serum osteocalcin level is associated with the mortality in Chinese patients with Fibrodysplasia ossificans progressiva aged ≤18 years at diagnosis.</pubmed_title><pmcid>PMC7060591</pmcid><funding_grant_id>81670805</funding_grant_id><funding_grant_id>81400834</funding_grant_id><funding_grant_id>81974105</funding_grant_id><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>She D</pubmed_authors><pubmed_authors>Zong G</pubmed_authors><pubmed_authors>Fang P</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serum osteocalcin level is associated with the mortality in Chinese patients with Fibrodysplasia ossificans progressiva aged ≤18 years at diagnosis.</name><description>&lt;h4>Background&lt;/h4>Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare genetic disorder characterized by extraskeletal heterotopic ossification. It is well recognized that FOP can lead to a devastating condition of disability. However, the mortality rate of FOP patients in China and risk factors for mortality are still largely unclear.&lt;h4>Methods&lt;/h4>We conducted a retrospective research on a cohort of 65 cases of FOP patients in China from 2008 to 2018. We reviewed medical records of these FOP patients to retrieve information such as date of birth/death, gender, clinical features, genotypes and biochemical parameters and analyze the correlation of these parameters with the mortality.&lt;h4>Results&lt;/h4>92.3% (60/65 cases) patients were classic FOP patients, 3.1% (2/65 cases) were FOP</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Mar</publication><modification>2026-04-16T21:07:50.062Z</modification><creation>2020-05-22T13:01:42Z</creation></dates><accession>S-EPMC7060591</accession><cross_references><pubmed>32143615</pubmed><doi>10.1186/s12891-020-3170-3</doi></cross_references></HashMap>