Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report
Abstract Background Generalized Arterial Calcification of Infancy (GACI) is a heritable ectopic mineralization disorder resulting in diffuse arterial calcifications and/or stenosis, mostly caused by mutations in the ENPP1 gene. Here we present a case report of GACI in a male infant with a new famili...
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doaj-b7932e7b7d5c4aeeb449e46d96c6982a2020-11-24T21:21:54ZengBMCBMC Pediatrics1471-24312018-07-011811510.1186/s12887-018-1198-4Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case reportIole Brunod0Barthélémy Tosello1Sophie Hassid2Catherine Gire3Laurent Thomachot4Michel Panuel5Pediatric and Neonatal Intensive Care Unit, Hôpital Nord, Assistance Publique-Hôpitaux de MarseilleDepartment of Neonatology, Hôpital Nord, Assistance Publique des Hôpitaux de Marseille (APHM)Pediatric and Neonatal Intensive Care Unit, Hôpital Nord, Assistance Publique-Hôpitaux de MarseilleDepartment of Neonatology, Hôpital Nord, Assistance Publique des Hôpitaux de Marseille (APHM)Pediatric and Neonatal Intensive Care Unit, Hôpital Nord, Assistance Publique-Hôpitaux de MarseilleAix Marseille Univ, CNRS, EFS, ADESAbstract Background Generalized Arterial Calcification of Infancy (GACI) is a heritable ectopic mineralization disorder resulting in diffuse arterial calcifications and/or stenosis, mostly caused by mutations in the ENPP1 gene. Here we present a case report of GACI in a male infant with a new familial mutation of the ENPP1 gene and the clinical outcome after biphosphonates therapy. Case presentation The clinical presentation was characterized by a severe early-onset of hypertension refractory to multiple therapy. To investigate this atypical hypertension, a renal Doppler ultra-sonography was performed and diffuse echo-bright arteries were detected; then a low-dose whole-body computed tomography demonstrated extensive arterial calcifications, suggesting GACI. A novel homozygous mutation c.784A > G (p.Ser262Gly) was detected in the ENPP1 gene. The infant was administered four courses of bisphosphonates: arterial calcifications were found to decrease but severe refractory hypertension was persistent. Although GACI can be a rapidly fatal illness and frequently results in death in infancy, the patient was 24 months of age at the time of writing this report. Conclusions Three points of interest: the first one is to remind clinicians of this rare and atypical etiology in neonates with severe hypertension and in fetuses with cardiomyopathy and non-immune hydrops fetalis. The second point is the identification of a novel mutation in the ENPP1 gene associated with a clinical presentation of GACI. The third point is the fairly favourable outcome of our patient after bisphosphonates therapy, with calcifications regression but not hypertension.http://link.springer.com/article/10.1186/s12887-018-1198-4ENPP1Generalized arterial calcification of infancyArterial calcificationNeonatal hypertension |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Iole Brunod Barthélémy Tosello Sophie Hassid Catherine Gire Laurent Thomachot Michel Panuel |
spellingShingle |
Iole Brunod Barthélémy Tosello Sophie Hassid Catherine Gire Laurent Thomachot Michel Panuel Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report BMC Pediatrics ENPP1 Generalized arterial calcification of infancy Arterial calcification Neonatal hypertension |
author_facet |
Iole Brunod Barthélémy Tosello Sophie Hassid Catherine Gire Laurent Thomachot Michel Panuel |
author_sort |
Iole Brunod |
title |
Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report |
title_short |
Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report |
title_full |
Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report |
title_fullStr |
Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report |
title_full_unstemmed |
Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report |
title_sort |
generalized arterial calcification of infancy with a novel enpp1 mutation: a case report |
publisher |
BMC |
series |
BMC Pediatrics |
issn |
1471-2431 |
publishDate |
2018-07-01 |
description |
Abstract Background Generalized Arterial Calcification of Infancy (GACI) is a heritable ectopic mineralization disorder resulting in diffuse arterial calcifications and/or stenosis, mostly caused by mutations in the ENPP1 gene. Here we present a case report of GACI in a male infant with a new familial mutation of the ENPP1 gene and the clinical outcome after biphosphonates therapy. Case presentation The clinical presentation was characterized by a severe early-onset of hypertension refractory to multiple therapy. To investigate this atypical hypertension, a renal Doppler ultra-sonography was performed and diffuse echo-bright arteries were detected; then a low-dose whole-body computed tomography demonstrated extensive arterial calcifications, suggesting GACI. A novel homozygous mutation c.784A > G (p.Ser262Gly) was detected in the ENPP1 gene. The infant was administered four courses of bisphosphonates: arterial calcifications were found to decrease but severe refractory hypertension was persistent. Although GACI can be a rapidly fatal illness and frequently results in death in infancy, the patient was 24 months of age at the time of writing this report. Conclusions Three points of interest: the first one is to remind clinicians of this rare and atypical etiology in neonates with severe hypertension and in fetuses with cardiomyopathy and non-immune hydrops fetalis. The second point is the identification of a novel mutation in the ENPP1 gene associated with a clinical presentation of GACI. The third point is the fairly favourable outcome of our patient after bisphosphonates therapy, with calcifications regression but not hypertension. |
topic |
ENPP1 Generalized arterial calcification of infancy Arterial calcification Neonatal hypertension |
url |
http://link.springer.com/article/10.1186/s12887-018-1198-4 |
work_keys_str_mv |
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