Propionic Acidemia with Novel Mutation Presenting as Recurrent Pancreatitis in a Child
Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities-such as hyperammonemia, metabolic acidosis, and ketosis-associated with complaints of v...
        Saved in:
      
    
          | Published in | Journal of Korean medical science Vol. 34; no. 47; pp. e303 - 6 | 
|---|---|
| Main Authors | , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Korea (South)
          The Korean Academy of Medical Sciences
    
        09.12.2019
     대한의학회  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1011-8934 1598-6357 1598-6357  | 
| DOI | 10.3346/jkms.2019.34.e303 | 
Cover
| Abstract | Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities-such as hyperammonemia, metabolic acidosis, and ketosis-associated with complaints of vomiting, feeding difficulties, and hypotonia during the neonatal period. However, in rare late-onset cases, mild or vague symptoms make the diagnosis more challenging. Even though acute pancreatitis is relatively uncommon in children, it can occur in association with PA. We present the case of a 4-year-old child who was admitted owing to the complaint of recurrent pancreatitis and had not previously been diagnosed with having metabolic disease. During inpatient treatment for acute pancreatitis, convulsions occurred with concomitant hyperammonemia, metabolic acidosis, coagulopathy, and shock 1 week after the administration of total parenteral nutrition. He was diagnosed to have PA after a metabolic work-up and confirmed to have novel mutation by molecular genetic analysis. Because children with PA may have acute pancreatitis, although rare, vomiting and abdominal pain should raise a suspicion of acute pancreatitis. On the contrary, even among children who have never been diagnosed with a metabolic disease, if a child has recurrent pancreatitis, metabolic pancreatitis caused by organic acidemia should be considered. | 
    
|---|---|
| AbstractList | Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities-such as hyperammonemia, metabolic acidosis, and ketosis-associated with complaints of vomiting, feeding difficulties, and hypotonia during the neonatal period. However, in rare late-onset cases, mild or vague symptoms make the diagnosis more challenging. Even though acute pancreatitis is relatively uncommon in children, it can occur in association with PA. We present the case of a 4-year-old child who was admitted owing to the complaint of recurrent pancreatitis and had not previously been diagnosed with having metabolic disease. During inpatient treatment for acute pancreatitis, convulsions occurred with concomitant hyperammonemia, metabolic acidosis, coagulopathy, and shock 1 week after the administration of total parenteral nutrition. He was diagnosed to have PA after a metabolic work-up and confirmed to have novel mutation by molecular genetic analysis. Because children with PA may have acute pancreatitis, although rare, vomiting and abdominal pain should raise a suspicion of acute pancreatitis. On the contrary, even among children who have never been diagnosed with a metabolic disease, if a child has recurrent pancreatitis, metabolic pancreatitis caused by organic acidemia should be considered. Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities-such as hyperammonemia, metabolic acidosis, and ketosis-associated with complaints of vomiting, feeding difficulties, and hypotonia during the neonatal period. However, in rare late-onset cases, mild or vague symptoms make the diagnosis more challenging. Even though acute pancreatitis is relatively uncommon in children, it can occur in association with PA. We present the case of a 4-year-old child who was admitted owing to the complaint of recurrent pancreatitis and had not previously been diagnosed with having metabolic disease. During inpatient treatment for acute pancreatitis, convulsions occurred with concomitant hyperammonemia, metabolic acidosis, coagulopathy, and shock 1 week after the administration of total parenteral nutrition. He was diagnosed to have PA after a metabolic work-up and confirmed to have novel mutation by molecular genetic analysis. Because children with PA may have acute pancreatitis, although rare, vomiting and abdominal pain should raise a suspicion of acute pancreatitis. On the contrary, even among children who have never been diagnosed with a metabolic disease, if a child has recurrent pancreatitis, metabolic pancreatitis caused by organic acidemia should be considered.Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities-such as hyperammonemia, metabolic acidosis, and ketosis-associated with complaints of vomiting, feeding difficulties, and hypotonia during the neonatal period. However, in rare late-onset cases, mild or vague symptoms make the diagnosis more challenging. Even though acute pancreatitis is relatively uncommon in children, it can occur in association with PA. We present the case of a 4-year-old child who was admitted owing to the complaint of recurrent pancreatitis and had not previously been diagnosed with having metabolic disease. During inpatient treatment for acute pancreatitis, convulsions occurred with concomitant hyperammonemia, metabolic acidosis, coagulopathy, and shock 1 week after the administration of total parenteral nutrition. He was diagnosed to have PA after a metabolic work-up and confirmed to have novel mutation by molecular genetic analysis. Because children with PA may have acute pancreatitis, although rare, vomiting and abdominal pain should raise a suspicion of acute pancreatitis. On the contrary, even among children who have never been diagnosed with a metabolic disease, if a child has recurrent pancreatitis, metabolic pancreatitis caused by organic acidemia should be considered. Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are diagnosed after the detection of metabolic abnormalities—such as hyperammonemia, metabolic acidosis, and ketosis—associated with complaints of vomiting, feeding difficulties, and hypotonia during the neonatal period. However, in rare late-onset cases, mild or vague symptoms make the diagnosis more challenging. Even though acute pancreatitis is relatively uncommon in children, it can occur in association with PA. We present the case of a 4-year-old child who was admitted owing to the complaint of recurrent pancreatitis and had not previously been diagnosed with having metabolic disease. During inpatient treatment for acute pancreatitis, convulsions occurred with concomitant hyperammonemia, metabolic acidosis, coagulopathy, and shock 1 week after the administration of total parenteral nutrition. He was diagnosed to have PA after a metabolic work-up and confirmed to have novel mutation by molecular genetic analysis. Because children with PA may have acute pancreatitis, although rare, vomiting and abdominal pain should raise a suspicion of acute pancreatitis. On the contrary, even among children who have never been diagnosed with a metabolic disease, if a child has recurrent pancreatitis, metabolic pancreatitis caused by organic acidemia should be considered. KCI Citation Count: 0  | 
    
| Author | Choe, Jae Young Kang, Ben Hwang, Su-Kyeong Min, So Yoon Choe, Byung-Ho Jang, Kyung Mi  | 
    
| AuthorAffiliation | 1 Department of Emergency Medicine, School of Medicine, Kyungpook National University, Daegu, Korea 4 Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea 3 Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea 2 Department of Pediatrics, Yeungnam University College of Medicine, Yeungnam University Hospital, Daegu, Korea  | 
    
| AuthorAffiliation_xml | – name: 2 Department of Pediatrics, Yeungnam University College of Medicine, Yeungnam University Hospital, Daegu, Korea – name: 1 Department of Emergency Medicine, School of Medicine, Kyungpook National University, Daegu, Korea – name: 4 Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea – name: 3 Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea  | 
    
| Author_xml | – sequence: 1 givenname: Jae Young orcidid: 0000-0002-4107-6621 surname: Choe fullname: Choe, Jae Young organization: Department of Emergency Medicine, School of Medicine, Kyungpook National University, Daegu, Korea – sequence: 2 givenname: Kyung Mi orcidid: 0000-0002-2226-9268 surname: Jang fullname: Jang, Kyung Mi organization: Department of Pediatrics, Yeungnam University College of Medicine, Yeungnam University Hospital, Daegu, Korea – sequence: 3 givenname: So Yoon orcidid: 0000-0002-6673-2568 surname: Min fullname: Min, So Yoon organization: Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea – sequence: 4 givenname: Su-Kyeong orcidid: 0000-0001-8294-7094 surname: Hwang fullname: Hwang, Su-Kyeong organization: Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea – sequence: 5 givenname: Ben orcidid: 0000-0002-8516-9803 surname: Kang fullname: Kang, Ben organization: Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea – sequence: 6 givenname: Byung-Ho orcidid: 0000-0001-9899-9120 surname: Choe fullname: Choe, Byung-Ho organization: Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea  | 
    
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31808324$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002529970$$DAccess content in National Research Foundation of Korea (NRF)  | 
    
| BookMark | eNqFUctu1DAUtVARfcAHsEFewiJTvxNvkEYjoJVaOqoKW8txnI47iT21k1b9-zqkvLqA1bV1z7nnnnMPwZ4P3gLwFqMFpUwc32z7tCAIywVlC0sRfQEOMJdVISgv9_IbYVxUkrJ9cJjSDUKEc0JfgX2KK1RRwg7A93UMOxe8M3BpXGN7p-G9Gzbwa7izHTwfBz3kNlxHm6wfnL-GOsFLa8YY8x-utTfRZszgEnQearjauK55DV62ukv2zVM9At8-f7panRRnF19OV8uzwjBKh0JqLttaYMyZNqatbWNqigQmrCp5yxqGiRW2xVxQZJqqRhjRBkkuy1K2oirpEfgwz_WxVVvjVNDuR70OahvV8vLqVAlSlgzLjCUzdvQ7_XCvu07tout1fFAYqSlQNQWqpkAVZWoKNJM-zqTdWPd5vew56t_ESe7vjnebLH6nhESIoWnD908DYrgdbRpU75KxXae9DWNWo4SUOHvGGfruT61fIj-vlQHlDDAxpBRtq4yb75OlXfdPG_gZ8__WHwHW97t8 | 
    
| CitedBy_id | crossref_primary_10_1186_s12920_022_01202_2 crossref_primary_10_1186_s13023_021_01685_9 crossref_primary_10_1186_s13023_025_03622_6 crossref_primary_10_1016_j_pharmthera_2023_108501 crossref_primary_10_1007_s00395_024_01066_w  | 
    
| Cites_doi | 10.5223/pghn.2017.20.1.61 10.1002/ajmg.a.32561 10.3345/kjp.2008.51.9.964 10.1053/j.gastro.2005.12.031 10.1007/BF02138781 10.1016/j.ymgme.2011.09.022 10.1186/1750-1172-8-6 10.1002/ajmg.a.31457 10.1016/S0022-3476(05)80562-1 10.1007/BF01953939 10.1136/pgmj.71.831.32 10.1016/S0022-3476(94)70311-6 10.1515/jpem-2013-0031 10.1016/S0022-3476(96)70383-9 10.1016/j.ymgme.2011.08.007 10.1097/MPG.0b013e3181132252 10.1016/S0022-3476(81)80004-2 10.1177/000992280404300908  | 
    
| ContentType | Journal Article | 
    
| Copyright | 2019 The Korean Academy of Medical Sciences. 2019 The Korean Academy of Medical Sciences. 2019 The Korean Academy of Medical Sciences  | 
    
| Copyright_xml | – notice: 2019 The Korean Academy of Medical Sciences. – notice: 2019 The Korean Academy of Medical Sciences. 2019 The Korean Academy of Medical Sciences  | 
    
| DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 5PM ADTOC UNPAY ACYCR  | 
    
| DOI | 10.3346/jkms.2019.34.e303 | 
    
| DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic PubMed Central (Full Participant titles) Unpaywall for CDI: Periodical Content Unpaywall Korean Citation Index  | 
    
| DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic  | 
    
| DatabaseTitleList | MEDLINE MEDLINE - Academic  | 
    
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: UNPAY name: Unpaywall url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/ sourceTypes: Open Access Repository  | 
    
| DeliveryMethod | fulltext_linktorsrc | 
    
| Discipline | Medicine | 
    
| EISSN | 1598-6357 | 
    
| EndPage | 6 | 
    
| ExternalDocumentID | oai_kci_go_kr_ARTI_6277419 10.3346/jkms.2019.34.e303 PMC6900407 31808324 10_3346_jkms_2019_34_e303  | 
    
| Genre | Case Reports | 
    
| GroupedDBID | --- 29K 2WC 3O- 5-W 53G 5GY 8JR 8XY 9ZL AAYXX ADBBV ADRAZ AENEX ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL CITATION CS3 D-I DIK DU5 E3Z EBS EF. EJD F5P FRP GROUPED_DOAJ GX1 HYE KQ8 M48 O5R O5S OK1 OVT PGMZT RNS RPM TR2 W2D XSB CGR CUY CVF ECM EIF NPM 7X8 5PM ADTOC UNPAY 08R ACYCR M~E  | 
    
| ID | FETCH-LOGICAL-c433t-9a59fb61154accfbedcb306124875f4d412e6ef15630cd8b0103d0959779f6873 | 
    
| IEDL.DBID | M48 | 
    
| ISSN | 1011-8934 1598-6357  | 
    
| IngestDate | Tue Nov 21 21:29:02 EST 2023 Sun Oct 26 04:01:14 EDT 2025 Tue Sep 30 16:56:34 EDT 2025 Thu Oct 02 10:44:48 EDT 2025 Mon Jul 21 05:37:08 EDT 2025 Tue Jul 01 01:45:02 EDT 2025 Thu Apr 24 23:07:21 EDT 2025  | 
    
| IsDoiOpenAccess | true | 
    
| IsOpenAccess | true | 
    
| IsPeerReviewed | true | 
    
| IsScholarly | true | 
    
| Issue | 47 | 
    
| Keywords | Propionic Acidemia Child Pancreatitis  | 
    
| Language | English | 
    
| License | 2019 The Korean Academy of Medical Sciences. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. cc-by-nc  | 
    
| LinkModel | DirectLink | 
    
| MergedId | FETCHMERGED-LOGICAL-c433t-9a59fb61154accfbedcb306124875f4d412e6ef15630cd8b0103d0959779f6873 | 
    
| Notes | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3  | 
    
| ORCID | 0000-0002-8516-9803 0000-0002-4107-6621 0000-0001-8294-7094 0000-0002-2226-9268 0000-0002-6673-2568 0000-0001-9899-9120  | 
    
| OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3346/jkms.2019.34.e303 | 
    
| PMID | 31808324 | 
    
| PQID | 2322710611 | 
    
| PQPubID | 23479 | 
    
| PageCount | 6 | 
    
| ParticipantIDs | nrf_kci_oai_kci_go_kr_ARTI_6277419 unpaywall_primary_10_3346_jkms_2019_34_e303 pubmedcentral_primary_oai_pubmedcentral_nih_gov_6900407 proquest_miscellaneous_2322710611 pubmed_primary_31808324 crossref_citationtrail_10_3346_jkms_2019_34_e303 crossref_primary_10_3346_jkms_2019_34_e303  | 
    
| ProviderPackageCode | CITATION AAYXX  | 
    
| PublicationCentury | 2000 | 
    
| PublicationDate | 2019-12-09 | 
    
| PublicationDateYYYYMMDD | 2019-12-09 | 
    
| PublicationDate_xml | – month: 12 year: 2019 text: 2019-12-09 day: 09  | 
    
| PublicationDecade | 2010 | 
    
| PublicationPlace | Korea (South) | 
    
| PublicationPlace_xml | – name: Korea (South) | 
    
| PublicationTitle | Journal of Korean medical science | 
    
| PublicationTitleAlternate | J Korean Med Sci | 
    
| PublicationYear | 2019 | 
    
| Publisher | The Korean Academy of Medical Sciences 대한의학회  | 
    
| Publisher_xml | – name: The Korean Academy of Medical Sciences – name: 대한의학회  | 
    
| References | Sass (10.3346/jkms.2019.34.e303_ref4) 2004; 43 van der Meer (10.3346/jkms.2019.34.e303_ref5) 1996; 155 Yoo (10.3346/jkms.2019.34.e303_ref2) 2006 Grünert (10.3346/jkms.2019.34.e303_ref11) 2013; 8 Lemire (10.3346/jkms.2019.34.e303_ref19) 1996; 128 Kahler (10.3346/jkms.2019.34.e303_ref8) 1994; 124 Sag (10.3346/jkms.2019.34.e303_ref9) 2017; 20 Bultron (10.3346/jkms.2019.34.e303_ref12) 2008; 47 Lehnert (10.3346/jkms.2019.34.e303_ref3) 1994; 153 Pena (10.3346/jkms.2019.34.e303_ref6) 2012; 105 Wolf (10.3346/jkms.2019.34.e303_ref14) 1981; 99 Kabadi (10.3346/jkms.2019.34.e303_ref18) 1995; 71 Chapman (10.3346/jkms.2019.34.e303_ref1) 2012; 105 Gilmore (10.3346/jkms.2019.34.e303_ref13) 2008; 146A Fortson (10.3346/jkms.2019.34.e303_ref15) 1995; 90 Rafique (10.3346/jkms.2019.34.e303_ref10) 2013; 26 Criddle (10.3346/jkms.2019.34.e303_ref16) 2006; 130 Walter (10.3346/jkms.2019.34.e303_ref20) 1990; 117 Debray (10.3346/jkms.2019.34.e303_ref17) 2006; 140 Lee (10.3346/jkms.2019.34.e303_ref7) 2008; 51  | 
    
| References_xml | – volume: 20 start-page: 61 issue: 1 year: 2017 ident: 10.3346/jkms.2019.34.e303_ref9 publication-title: Pediatr Gastroenterol Hepatol Nutr doi: 10.5223/pghn.2017.20.1.61 – volume: 146A start-page: 3090 issue: 23 year: 2008 ident: 10.3346/jkms.2019.34.e303_ref13 publication-title: Am J Med Genet A doi: 10.1002/ajmg.a.32561 – volume-title: Epidemiologic Research of Genetic and Metabolic Disease in Korea year: 2006 ident: 10.3346/jkms.2019.34.e303_ref2 – volume: 51 start-page: 964 issue: 9 year: 2008 ident: 10.3346/jkms.2019.34.e303_ref7 publication-title: Korean J Pediatr doi: 10.3345/kjp.2008.51.9.964 – volume: 130 start-page: 781 issue: 3 year: 2006 ident: 10.3346/jkms.2019.34.e303_ref16 publication-title: Gastroenterology doi: 10.1053/j.gastro.2005.12.031 – volume: 153 start-page: S68 issue: 7 year: 1994 ident: 10.3346/jkms.2019.34.e303_ref3 publication-title: Eur J Pediatr doi: 10.1007/BF02138781 – volume: 105 start-page: 5 issue: 1 year: 2012 ident: 10.3346/jkms.2019.34.e303_ref6 publication-title: Mol Genet Metab doi: 10.1016/j.ymgme.2011.09.022 – volume: 8 start-page: 6 issue: 1 year: 2013 ident: 10.3346/jkms.2019.34.e303_ref11 publication-title: Orphanet J Rare Dis doi: 10.1186/1750-1172-8-6 – volume: 140 start-page: 2330 issue: 21 year: 2006 ident: 10.3346/jkms.2019.34.e303_ref17 publication-title: Am J Med Genet A doi: 10.1002/ajmg.a.31457 – volume: 117 start-page: 338 issue: 2 Pt 1 year: 1990 ident: 10.3346/jkms.2019.34.e303_ref20 publication-title: J Pediatr doi: 10.1016/S0022-3476(05)80562-1 – volume: 155 start-page: 205 issue: 3 year: 1996 ident: 10.3346/jkms.2019.34.e303_ref5 publication-title: Eur J Pediatr doi: 10.1007/BF01953939 – volume: 71 start-page: 32 issue: 831 year: 1995 ident: 10.3346/jkms.2019.34.e303_ref18 publication-title: Postgrad Med J doi: 10.1136/pgmj.71.831.32 – volume: 124 start-page: 239 issue: 2 year: 1994 ident: 10.3346/jkms.2019.34.e303_ref8 publication-title: J Pediatr doi: 10.1016/S0022-3476(94)70311-6 – volume: 26 start-page: 497 issue: 5-6 year: 2013 ident: 10.3346/jkms.2019.34.e303_ref10 publication-title: J Pediatr Endocrinol Metab doi: 10.1515/jpem-2013-0031 – volume: 128 start-page: 589 issue: 4 year: 1996 ident: 10.3346/jkms.2019.34.e303_ref19 publication-title: J Pediatr doi: 10.1016/S0022-3476(96)70383-9 – volume: 105 start-page: 3 issue: 1 year: 2012 ident: 10.3346/jkms.2019.34.e303_ref1 publication-title: Mol Genet Metab doi: 10.1016/j.ymgme.2011.08.007 – volume: 90 start-page: 2134 issue: 12 year: 1995 ident: 10.3346/jkms.2019.34.e303_ref15 publication-title: Am J Gastroenterol – volume: 47 start-page: 370 issue: 3 year: 2008 ident: 10.3346/jkms.2019.34.e303_ref12 publication-title: J Pediatr Gastroenterol Nutr doi: 10.1097/MPG.0b013e3181132252 – volume: 99 start-page: 835 issue: 6 year: 1981 ident: 10.3346/jkms.2019.34.e303_ref14 publication-title: J Pediatr doi: 10.1016/S0022-3476(81)80004-2 – volume: 43 start-page: 837 issue: 9 year: 2004 ident: 10.3346/jkms.2019.34.e303_ref4 publication-title: Clin Pediatr (Phila) doi: 10.1177/000992280404300908  | 
    
| SSID | ssj0025523 | 
    
| Score | 2.2412372 | 
    
| Snippet | Propionic acidemia (PA) is a rare organic acidemia resulting from a deficiency of the mitochondrial enzyme propionyl-coenzyme A carboxylase. Most cases are... | 
    
| SourceID | nrf unpaywall pubmedcentral proquest pubmed crossref  | 
    
| SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source  | 
    
| StartPage | e303 | 
    
| SubjectTerms | Case Report Child, Preschool Humans Male Mutation Pancreatitis - etiology Propionic Acidemia - complications Propionic Acidemia - diagnosis Propionic Acidemia - genetics Recurrence 의학일반  | 
    
| SummonAdditionalLinks | – databaseName: Unpaywall dbid: UNPAY link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELbYrgRceC-ElwziBEq2iZ2HjxVLtSxqFbEULSfLdmwoLUnUJqDl1-Nx0kK1CASnKMrElj1jz8v-BqFnWQEoYIz5olCFTzXTvhgSgK00JjUmMcIh8E2myfGMnpzFZz8Dbp8XX9Yuf396Xop6rQ-PRCMO86Oxe4I-PXkzOXVkPqG-thtwUBdmD-0nsbXFB2h_Ns1HH1yKMwx9q4xdWjlmmQ_Aa11akxBIa0JPVvuxgNAA2tlRTHvlyvzO5rx4dPJKW9bi_JtYLn_RS-PriG9u93THURZB28hAfb8I9vifQ76BrvUmKx51MnYTXdLlLXR50iflb6P3-aqqIayr8Ei5erMCQ3gXT6uveoknbZftx3l308nqSizW-C0E-gEaCudW8Jzp2szXeF5igR3e8h00G7969_LY78s1-IoS0vhMxMzIBPB9hFJG2kmSBCwo8IkMLWgY6USbEBDJVJFJqDBRQBgyTZlJspQcoEFZlfoewmxIJY1DVcg4oqnMhCQqY8Mikjo0ls8eGm54xVWPZQ4lNZbc-jTAXg7TxYG9nFAOc-ah59tf6g7I40_ET60A8IWac4DfhufHii9W3DoZr3kSWZs5ZB56spEPbtckJFpEqavWNmV3yRR87dBDdzt52fZp91Br9UbUQ-mOJG0JoMPdL-X8k8P9ThhsuamHXmxl7u9Duf9P1A_QVXh153XYQzRoVq1-ZK2uRj7ul9YPjqYpRw priority: 102 providerName: Unpaywall  | 
    
| Title | Propionic Acidemia with Novel Mutation Presenting as Recurrent Pancreatitis in a Child | 
    
| URI | https://www.ncbi.nlm.nih.gov/pubmed/31808324 https://www.proquest.com/docview/2322710611 https://pubmed.ncbi.nlm.nih.gov/PMC6900407 http://jkms.org/Synapse/Data/PDFData/0063JKMS/jkms-34-e303.pdf https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002529970  | 
    
| UnpaywallVersion | publishedVersion | 
    
| Volume | 34 | 
    
| hasFullText | 1 | 
    
| inHoldings | 1 | 
    
| isFullTextHit | |
| isPrint | |
| ispartofPNX | Journal of Korean Medical Science, 2019, 34(47), , pp.1-6 | 
    
| journalDatabaseRights | – providerCode: PRVAFT databaseName: Open Access Digital Library customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: KQ8 dateStart: 19860101 isFulltext: true titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html providerName: Colorado Alliance of Research Libraries – providerCode: PRVAON databaseName: DOAJ Directory of Open Access Journals customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: DOA dateStart: 20100101 isFulltext: true titleUrlDefault: https://www.doaj.org/ providerName: Directory of Open Access Journals – providerCode: PRVBFR databaseName: Free Medical Journals customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: DIK dateStart: 19860101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: GX1 dateStart: 0 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research – providerCode: PRVERR databaseName: KoreaMed Open Access customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: 5-W dateStart: 19860101 isFulltext: true titleUrlDefault: https://koreamed.org/journals providerName: Korean Association of Medical Journal Editors – providerCode: PRVAQN databaseName: PubMed Central customDbUrl: eissn: 1598-6357 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: RPM dateStart: 19860101 isFulltext: true titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/ providerName: National Library of Medicine – providerCode: PRVFZP databaseName: Scholars Portal Journals: Open Access customDbUrl: eissn: 1598-6357 dateEnd: 20250831 omitProxy: true ssIdentifier: ssj0025523 issn: 1011-8934 databaseCode: M48 dateStart: 19860901 isFulltext: true titleUrlDefault: http://journals.scholarsportal.info providerName: Scholars Portal  | 
    
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3fb9MwELbGJgEvEz9HBlQG8QRKVcduEj8gVCGmDdSqQhSNJ8t2bKgakpK2wP577pI0oqICnvKQ2JbPZ993d853hDxLM2QBkzLUmc1C4aQL9YAjbaX3ifex1zUD33gSn8_E28vh5QHZlrdqBbja69phPalZlfd_frt6BRv-JXqcHDOUi69IvM1kn4u-48j9eQSGSmIlh7HokgoAnqPmvj1jIZhp0SQ593exY6auFZXfh0D_vEh5Y1Ms9dUPnee_WamzW-S4hZd01OjDbXLgijvk-rhNoN8lH6dVucQQrKUjW9eG1RRDsXRSfnc5HW-azDydNn8lgV2jekXfY1AeaZzoFJSkhpnr-YrOC6ppzY18j8zO3nx4fR62pRVCKzhfh1IPpTcxcvFoa72BKRiOaAf9Fy8ywSIXO8-QPcxmqcFqEBmGDJNE-jhN-H1yWJSFe0CoHAgjhsxmZhiJxKTacJvKQRYZxzz4RwEZbCWpbMs7juUvcgX-BwpfofAVCl9xoVD4AXneNVk2pBt_-_gpLI9a2LlCqmx8fi7VolLgEFyoOAJ8y2RAnmxXT8H-waSILly5ga7gREvQL2YBOWlWsxsTzjtAqJEISLKzzt0HOODum2L-pebojiUej0lAXnQa8e-pnP7PVB6Sm9imvlIjH5HDdbVxjwEYrU0PXIKLd706rNCrVb9HjmaT6ejTLx8XDtU | 
    
| linkProvider | Scholars Portal | 
    
| linkToUnpaywall | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELbYrgRceC-ElwziBEq2iZ2HjxVLtSxqFbEULSfLdmwoLUnUJqDl1-Nx0kK1CASnKMrElj1jz8v-BqFnWQEoYIz5olCFTzXTvhgSgK00JjUmMcIh8E2myfGMnpzFZz8Dbp8XX9Yuf396Xop6rQ-PRCMO86Oxe4I-PXkzOXVkPqG-thtwUBdmD-0nsbXFB2h_Ns1HH1yKMwx9q4xdWjlmmQ_Aa11akxBIa0JPVvuxgNAA2tlRTHvlyvzO5rx4dPJKW9bi_JtYLn_RS-PriG9u93THURZB28hAfb8I9vifQ76BrvUmKx51MnYTXdLlLXR50iflb6P3-aqqIayr8Ei5erMCQ3gXT6uveoknbZftx3l308nqSizW-C0E-gEaCudW8Jzp2szXeF5igR3e8h00G7969_LY78s1-IoS0vhMxMzIBPB9hFJG2kmSBCwo8IkMLWgY6USbEBDJVJFJqDBRQBgyTZlJspQcoEFZlfoewmxIJY1DVcg4oqnMhCQqY8Mikjo0ls8eGm54xVWPZQ4lNZbc-jTAXg7TxYG9nFAOc-ah59tf6g7I40_ET60A8IWac4DfhufHii9W3DoZr3kSWZs5ZB56spEPbtckJFpEqavWNmV3yRR87dBDdzt52fZp91Br9UbUQ-mOJG0JoMPdL-X8k8P9ThhsuamHXmxl7u9Duf9P1A_QVXh153XYQzRoVq1-ZK2uRj7ul9YPjqYpRw | 
    
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Propionic+Acidemia+with+Novel+Mutation+Presenting+as+Recurrent+Pancreatitis+in+a+Child&rft.jtitle=Journal+of+Korean+medical+science&rft.au=%EC%B5%9C%EC%9E%AC%EC%98%81&rft.au=%EC%9E%A5%EA%B2%BD%EB%AF%B8&rft.au=%EB%AF%BC%EC%86%8C%EC%9C%A4&rft.au=%ED%99%A9%EC%88%98%EA%B2%BD&rft.date=2019-12-09&rft.pub=%EB%8C%80%ED%95%9C%EC%9D%98%ED%95%99%ED%9A%8C&rft.issn=1011-8934&rft.eissn=1598-6357&rft.spage=1&rft.epage=6&rft_id=info:doi/10.3346%2Fjkms.2019.34.e303&rft.externalDBID=n%2Fa&rft.externalDocID=oai_kci_go_kr_ARTI_6277419 | 
    
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1011-8934&client=summon | 
    
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1011-8934&client=summon | 
    
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1011-8934&client=summon |