Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. (21st April 2015)
- Record Type:
- Journal Article
- Title:
- Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. (21st April 2015)
- Main Title:
- Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE
- Authors:
- Richer, Julie
Daoud, Hussein
Geier, Pavel
Jarinova, Olga
Carson, Nancy
Feberova, Jana
Fadfel, Nadya Ben
Unrau, Jennifer
Bareke, Eric
Khatchadourian, Karine
Bulman, Dennis E
Majewski, Jacek
Boycott, Kym M
Dyment, David A - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga37067-sec-0001" sec-type="section"> <p>We present the investigation and management of a premature, hypotensive neonate born after a pregnancy complicated by anhydramnios to highlight the impact of early and informed management for rare kidney disease. Vasopressin was used to successfully treat refractory hypotension and anuria in the neonate born at 27 weeks of gestation. Next generation sequencing of a targeted panel of genes was then performed in the neonate and parents. Subsequently, two compound heterozygous deletions leading to frameshift mutations were identified in the angiotensin 1‐converting enzyme gene <italic>ACE</italic>; exon 5:c.820_821delAG (p.Arg274Glyfs*117) and exon24: c.3521delG (p.Gly1174Alafs*12), consistent with a diagnosis of renal tubular dysgenesis. In light of the molecular diagnosis, identification, and treatment of associated low aldosterone level resulted in further improvement in renal function and only mild residual chronic renal failure is present at 14 months of age. Truncating alterations in ACE most often result in fetal demise during gestation or in the first days of life and typically as a result of the Potter sequence. The premature delivery, and serendipitous early treatment with vasopressin, and then later fludrocortisone, resulted in an optimal outcome in an otherwise lethal condition. © 2015 Wiley Periodicals, Inc.</p><abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga37067-sec-0001" sec-type="section"> <p>We present the investigation and management of a premature, hypotensive neonate born after a pregnancy complicated by anhydramnios to highlight the impact of early and informed management for rare kidney disease. Vasopressin was used to successfully treat refractory hypotension and anuria in the neonate born at 27 weeks of gestation. Next generation sequencing of a targeted panel of genes was then performed in the neonate and parents. Subsequently, two compound heterozygous deletions leading to frameshift mutations were identified in the angiotensin 1‐converting enzyme gene <italic>ACE</italic>; exon 5:c.820_821delAG (p.Arg274Glyfs*117) and exon24: c.3521delG (p.Gly1174Alafs*12), consistent with a diagnosis of renal tubular dysgenesis. In light of the molecular diagnosis, identification, and treatment of associated low aldosterone level resulted in further improvement in renal function and only mild residual chronic renal failure is present at 14 months of age. Truncating alterations in ACE most often result in fetal demise during gestation or in the first days of life and typically as a result of the Potter sequence. The premature delivery, and serendipitous early treatment with vasopressin, and then later fludrocortisone, resulted in an optimal outcome in an otherwise lethal condition. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of medical genetics. Volume 167:Number 7(2015:Jul.)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 167:Number 7(2015:Jul.)
- Issue Display:
- Volume 167, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 167
- Issue:
- 7
- Issue Sort Value:
- 2015-0167-0007-0000
- Page Start:
- 1654
- Page End:
- 1658
- Publication Date:
- 2015-04-21
- Subjects:
- Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.37067 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3135.xml