{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,21]],"date-time":"2026-03-21T07:36:55Z","timestamp":1774078615683,"version":"3.50.1"},"reference-count":10,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2026,3,17]],"date-time":"2026-03-17T00:00:00Z","timestamp":1773705600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Obstet Med"],"abstract":"<jats:p>Glycogen Storage Disease Type IIIA (GSD IIIA) is a rare autosomal recessive metabolic disorder affecting the liver, skeletal muscle, and heart. The physiological changes of pregnancy exacerbate the underlying metabolic disturbances of this condition, complicating maternal and fetal outcomes. We present the case of a 22-year-old woman with GSD IIIA who experienced a successful pregnancy and delivery through comprehensive multidisciplinary management, including metabolic, obstetric, dietary, anaesthetic, and neonatal care. This case contributes to the limited but growing body of literature on pregnancy in GSD IIIA and highlights the critical importance of personalized, team-based care in rare metabolic diseases.<\/jats:p>","DOI":"10.1177\/1753495x261431284","type":"journal-article","created":{"date-parts":[[2026,3,17]],"date-time":"2026-03-17T10:31:09Z","timestamp":1773743469000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Successful multidisciplinary management of pregnancy in a woman with glycogen storage disease type IIIA"],"prefix":"10.1177","author":[{"given":"Loai A.","family":"Shakerdi","sequence":"first","affiliation":[{"name":"Mater Misericordiae University Hospital, Dublin, Ireland"},{"name":"University College Dublin"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-4857-1846","authenticated-orcid":false,"given":"Halima","family":"Mshelia","sequence":"additional","affiliation":[{"name":"Cork University Hospital"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abrar","family":"Al Zaher","sequence":"additional","affiliation":[{"name":"Cork University Hospital"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rawia","family":"Debo","sequence":"additional","affiliation":[{"name":"The Coombe Hospital"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sarah","family":"Connellan","sequence":"additional","affiliation":[{"name":"Mater Misericordiae University Hospital, Dublin, Ireland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cathy","family":"Newman Thacker","sequence":"additional","affiliation":[{"name":"Mater Misericordiae University Hospital, Dublin, Ireland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mairead","family":"O\u2019Riordan","sequence":"additional","affiliation":[{"name":"Cork University Hospital"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James J.","family":"O\u2019Byrne","sequence":"additional","affiliation":[{"name":"Mater Misericordiae University Hospital, Dublin, Ireland"},{"name":"Trinity College Dublin"},{"name":"University College Dublin (UCD)"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Claire M.","family":"McCarthy","sequence":"additional","affiliation":[{"name":"Cork University Hospital"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2026,3,17]]},"reference":[{"key":"e_1_3_3_2_2","first-page":"72","article-title":"Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency","volume":"26","author":"Lucchiari S","year":"2007","unstructured":"Lucchiari S, Santoro D, Pagliarani S, et al. Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency. Acta Myol 2007; 26: 72\u201374.","journal-title":"Acta Myol"},{"key":"e_1_3_3_3_2","volume-title":"Urea cycle disorders overview","author":"Schreuder AB","year":"1993","unstructured":"Schreuder AB, Rossi A, Grunert SC, et al. Glycogen Storage Disease Type III. In: Adam MP, Ardinger HH, Pagon RA, Bird TD, Dolan CR, Fong CT, Rjh S, Stephens K (eds) Urea cycle disorders overview. Seattle, WA: GeneReviews((R)), 1993."},{"key":"e_1_3_3_4_2","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-016-9932-2"},{"key":"e_1_3_3_5_2","first-page":"216","article-title":"Glycogen storage disease type IIIa in pregnant women: a guide to management","volume":"63","author":"Beneru D","year":"2022","unstructured":"Beneru D, Tchan MC, Billmore K, et al. Glycogen storage disease type IIIa in pregnant women: a guide to management. 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