Refractory congestive heart failure following delayed pericardectomy in a 12-year-old child with Mulibrey nanism due to a novel mutation in TRIM37

Kumpf, M; Hämäläinen, RH; Hofbeck, M; Baden, W

HERO ID

3539537

Reference Type

Journal Article

Year

2013

Language

English

PMID

23385855

HERO ID 3539537
In Press No
Year 2013
Title Refractory congestive heart failure following delayed pericardectomy in a 12-year-old child with Mulibrey nanism due to a novel mutation in TRIM37
Authors Kumpf, M; Hämäläinen, RH; Hofbeck, M; Baden, W
Journal European Journal of Pediatrics
Volume 172
Issue 10
Page Numbers 1415-1418
Abstract <strong>UNLABELLED: </strong>Mulibrey nanism (MUL) is a rare autosomal recessive disorder with severe primordial growth retardation and multiorgan involvement, caused by mutations in TRIM37. Early clinical detection is important since more than 50 % of the patients develop congestive heart failure. We report a 12-year-old patient who presented in infancy with severe growth retardation, dysmorphic features, and cleft palate. Clinical diagnosis of MUL was established at the age of 5 years. Postmortem, molecular diagnostic confirmed MUL as a novel 1-bp deletion (c.1233delA) in exon 14 of the TRIM37 coding region. Cardiac examination at the age of 6 years revealed constrictive pericarditis with significant elevation of atrial filling pressures, consecutive hepatomegaly, and protein loosing enteropathy. Since the parents refused pericardectomy, surgery was delayed until the age of 12 years, when congestive heart failure deteriorated. Despite pericardectomy, the boy died from persistent right heart failure.<br /><br /><strong>CONCLUSION: </strong>Our report underlines the necessity of early clinical diagnosis of Mulibrey nanism. Careful cardiologic examination is required to detect constrictive pericarditis, which is a major factor of mortality in these patients. Pericardectomy should be performed early, to avoid sequelae of persisting congestive heart failure.
Doi 10.1007/s00431-013-1962-2
Pmid 23385855
Wosid WOS:000324816900020
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English