{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T19:25:11Z","timestamp":1787772311806,"version":"build-2784847793"},"reference-count":10,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2021,4]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Restrictive cardiomyopathy is an unusual form of cardiomyopathy accounting only for 2%\u20135% of all pediatric cardiomyopathies. It is mostly idiopathic. Gaucher disease in association with restrictive cardiomyopathy is extremely rare. We herein report a case of cardiac failure in an 8-year-old male child caused by restrictive cardiomyopathy. Pathogenesis of which was attributed to Gaucher disease. In any case of restrictive cardiomyopathy, Gaucher disease should be included in differential diagnosis and investigated accordingly.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/aam.aam_64_18","type":"journal-article","created":{"date-parts":[[2024,5,22]],"date-time":"2024-05-22T12:48:06Z","timestamp":1716382086000},"page":"138-140","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":7,"title":["Restrictive Cardiomyopathy"],"prefix":"10.4103","volume":"20","author":[{"given":"Soumi","family":"Kundu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Malay Kumar","family":"Dasgupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Biswajit","family":"Majumder","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sayan","family":"Pradhan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-12-20240831","doi-asserted-by":"crossref","first-page":"1639","DOI":"10.1056\/NEJMoa021737","article-title":"The epidemiology of childhood cardiomyopathy in Australia","volume":"348","author":"Nugent","year":"2003","journal-title":"N Engl J Med"},{"key":"R2-12-20240831","doi-asserted-by":"crossref","first-page":"1647","DOI":"10.1056\/NEJMoa021715","article-title":"The incidence of pediatric cardiomyopathy in two regions of the United States","volume":"348","author":"Lipshultz","year":"2003","journal-title":"N Engl J Med"},{"key":"R3-12-20240831","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1016\/S1053-2498(01)00400-4","article-title":"Cardiac transplantation for pediatric restrictive cardiomyopathy: Presentation, evaluation, and short-term outcome","volume":"21","author":"Kimberling","year":"2002","journal-title":"J Heart Lung Transplant"},{"key":"R4-12-20240831","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1177\/2042018810384429","article-title":"Therapeutic approaches for lysosomal storage diseases","volume":"1","author":"Pastores","year":"2010","journal-title":"Ther Adv Endocrinol Metab"},{"key":"R5-12-20240831","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1016\/j.ppedcard.2007.08.013","article-title":"Diagnostic approaches to pediatric cardiomyopathy of metabolic genetic etiologies and their relation to therapy","volume":"24","author":"Cox","year":"2007","journal-title":"Prog Pediatr Cardiol"},{"key":"R6-12-20240831","doi-asserted-by":"crossref","first-page":"1000","DOI":"10.1016\/S0140-6736(95)91688-1","article-title":"Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype","volume":"346","author":"Abrahamov","year":"1995","journal-title":"Lancet"},{"key":"R7-12-20240831","doi-asserted-by":"crossref","first-page":"56","DOI":"10.1007\/BF00788233","article-title":"Gaucher's disease with mitral and aortic involvement: Echocardiographic findings","volume":"13","author":"Sara\u00e7lar","year":"1992","journal-title":"Pediatr Cardiol"},{"key":"R8-12-20240831","first-page":"211","article-title":"Hydrocephalus, corneal opacities, deafness, left ventricle hypertrophy, clinodactyly in an adolescent patient. A new syndrome associated with glucocerebrosidase deficiency","volume":"6","author":"Erduran","year":"1995","journal-title":"Genet Couns"},{"key":"R9-12-20240831","doi-asserted-by":"crossref","first-page":"740","DOI":"10.1136\/jmg.32.9.740","article-title":"Unusual expression of gaucher's disease: Cardiovascular calcifications in three sibs homozygous for the D409H mutation","volume":"32","author":"Chab\u00e1s","year":"1995","journal-title":"J Med Genet"},{"key":"R10-12-20240831","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1186\/s13256-016-1147-5","article-title":"Combination therapy in a patient with chronic neuronopathic gaucher disease: A case report","volume":"11","author":"Ceravolo","year":"2017","journal-title":"J Med Case Rep"}],"container-title":["Annals of African Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_64_18","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T18:37:54Z","timestamp":1787769474000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_64_18"}},"subtitle":["A Rare Presentation of Gaucher Disease"],"short-title":[],"issued":{"date-parts":[[2021,4]]},"references-count":10,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2021]]}},"URL":"https:\/\/doi.org\/10.4103\/aam.aam_64_18","relation":{},"ISSN":["1596-3519"],"issn-type":[{"value":"1596-3519","type":"print"}],"subject":[],"published":{"date-parts":[[2021,4]]}}}