{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,11]],"date-time":"2025-10-11T13:23:44Z","timestamp":1760189024399},"reference-count":7,"publisher":"BMJ","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Archives of Disease in Childhood"],"published-print":{"date-parts":[[1973,1,1]]},"DOI":"10.1136\/adc.48.1.63","type":"journal-article","created":{"date-parts":[[2008,12,22]],"date-time":"2008-12-22T21:05:14Z","timestamp":1229979914000},"page":"63-66","source":"Crossref","is-referenced-by-count":26,"title":["Familia neuroblastoma: report of two sib pairs."],"prefix":"10.1136","volume":"48","author":[{"given":"J","family":"Wagget","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Aherne","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"W","family":"Aherne","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"1230","DOI":"10.1056\/NEJM196712072772304","article-title":"Familial neuroblastoma. Report of a kindred with multiple disorders including neuroblastomas in four siblings","volume":"277","author":"Chatten, J.; Voorhess, M.L.","year":"1967","unstructured":"Chatten, J., and Voorhess, M. L. (1967). Familial neuroblastoma. Report of a kindred with multiple disorders including neuroblastomas in four siblings. New England journal of Medicine, 277, 1230.","journal-title":"New England journal of Medicine"},{"key":"ref_2","first-page":"35","article-title":"Neuroblastoma of adrenal medulla in siblings","volume":"42","author":"Dodge, H.J.; Benner, M.C.","year":"1945","unstructured":"Dodge, H. J., and Benner, M. C. (1945). Neuroblastoma of adrenal medulla in siblings. Rocky Mountain Medical Journal, 42, 35.","journal-title":"Rocky Mountain Medical Journal"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1016\/S0022-3476(72)80456-6","article-title":"Familial neuroblastoma: report of a kindred with a high incidence of infantile tumors","volume":"80","author":"Hardy, P.C.; Nesbit, M.E.","year":"1972","unstructured":"Hardy, P. C., and Nesbit, M. E. (1972). Familial neuroblastoma: report of a kindred with a high incidence of infantile tumors. Jtournal of Pediatrics, 80, 74.","journal-title":"Jtournal of Pediatrics"},{"key":"ref_4","first-page":"355","article-title":"Ganglioneuroblastome als erbliche Systemerkrankung des sympathicus. Beitrage zurpathologischen Anatomie und zur allgemeinen","volume":"111","author":"Zimmerman, J.","year":"1951","unstructured":"Zimmerman, J. (1951). Ganglioneuroblastome als erbliche Systemerkrankung des sympathicus. Beitrage zurpathologischen Anatomie und zur allgemeinen Pathologie, 111, 355.","journal-title":"Pathologie"},{"key":"ref_5","first-page":"and","article-title":"aetiology in which there occurs a diffuse thickening up of the mural endocardium associated in most cases with myocardial hypertrophy and leading to early death'. Andersen and Kelly","author":"Sellers, Keith","year":"1956","unstructured":"aetiology in which there occurs a diffuse thickening up of the mural endocardium associated in most cases with myocardial hypertrophy and leading to early death'. Andersen and Kelly (1956) divided their series of endocardial fibroelastosis into the common variety associated with other congenital cardiac anomalies and the rarer primary form without such anomalies, and found a familial incidence in 23% of the primary variety. Forfar et al. (1964), reviewing 72 cases of endocardial fibroelastosis, found multiple familial incidence only in the primary group which accounted for 22% of their cases. A familial incidence has also been described in the primary form by Dordick (1951), Winter et al. (1960), and Sellers, Keith, and Manning (1964).","journal-title":"Forfar et al; divided their series of endocardial fibroelastosis into the common variety associated with other congenital cardiac anomalies and the rarer primary form without such anomalies, and found a familial incidence in 23% of the primary variety"},{"key":"ref_6","article-title":"A recent and attractive view is that EFE is a secondary response in certain individuals either to an intrinsic inherited myocardial defect, which results in inefficient myocardial function, or to grossly abnormal haemodynamics associated with a congenitally malformed heart","volume-title":"This view accords well with the clinical and haemodynamic findings in the natural history of primary and secondary varieties","year":"1964","unstructured":"A recent and attractive view is that EFE is a secondary response in certain individuals either to an intrinsic inherited myocardial defect, which results in inefficient myocardial function, or to grossly abnormal haemodynamics associated with a congenitally malformed heart (Moller et al., 1964). This view accords well with the clinical and haemodynamic findings in the natural history of primary and secondary varieties."},{"key":"ref_7","article-title":"Primary endocardial fibroelastosis An inherited condition The name endocardial fibroelastosis (EFE) was introduced by Weinberg and Himelfarb in 1943, though the condition had been described under other names. Gowing","volume-title":"defined endocardial fibroelastosis as a 'congenital condition of unknown Family I. There were 3 children in this family. The first child (Case 1, female) had the typical clinical picture of EFE in infancy but remains well on digoxin, though with reduced exercise tolerance. Cardiac catheterization has not been carried out. The second child (female) is apparently normal. The third child (Case 2, male) died in infancy after a brief but typical illness, and primary EFE was confirmed at necropsy. There is no family history of heart disease","year":"1953","unstructured":"Primary endocardial fibroelastosis An inherited condition The name endocardial fibroelastosis (EFE) was introduced by Weinberg and Himelfarb in 1943, though the condition had been described under other names. Gowing (1953) defined endocardial fibroelastosis as a 'congenital condition of unknown Family I. There were 3 children in this family. The first child (Case 1, female) had the typical clinical picture of EFE in infancy but remains well on digoxin, though with reduced exercise tolerance. Cardiac catheterization has not been carried out. The second child (female) is apparently normal. The third child (Case 2, male) died in infancy after a brief but typical illness, and primary EFE was confirmed at necropsy. There is no family history of heart disease."}],"container-title":["Archives of Disease in Childhood"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/adc.48.1.63","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T08:58:31Z","timestamp":1601110711000},"score":1,"resource":{"primary":{"URL":"https:\/\/adc.bmj.com\/lookup\/doi\/10.1136\/adc.48.1.63"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1973,1,1]]},"references-count":7,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1973,1,1]]}},"URL":"https:\/\/doi.org\/10.1136\/adc.48.1.63","relation":{},"ISSN":["0003-9888","1468-2044"],"issn-type":[{"value":"0003-9888","type":"print"},{"value":"1468-2044","type":"electronic"}],"subject":[],"published":{"date-parts":[[1973,1,1]]}}}