Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. Issue 1 (26th October 2020)
- Record Type:
- Journal Article
- Title:
- Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. Issue 1 (26th October 2020)
- Main Title:
- Variants in NAA15 cause pediatric hypertrophic cardiomyopathy
- Authors:
- Ritter, Alyssa
Berger, Justin H.
Deardorff, Matthew
Izumi, Kosuke
Lin, Kimberly Y.
Medne, Livija
Ahrens‐Nicklas, Rebecca C. - Abstract:
- Abstract: The NatA N‐acetyltransferase complex is important for cotranslational protein modification and regulation of multiple cellular processes. The NatA complex includes the core components of NAA10, the catalytic subunit, and NAA15, the auxiliary component. Both NAA10 and NAA15 have been associated with neurodevelopmental disorders with overlapping clinical features, including variable intellectual disability, dysmorphic facial features, and, less commonly, congenital anomalies such as cleft lip or palate. Cardiac arrhythmias, including long QT syndrome, ventricular tachycardia, and ventricular fibrillation were among the first reported cardiac manifestations in patients with NAA10‐related syndrome. Recently, three individuals with NAA10‐related syndrome have been reported to also have hypertrophic cardiomyopathy (HCM). The general and cardiac phenotypes of NAA15‐related syndrome are not as well described as NAA10‐related syndrome. Congenital heart disease, including ventricular septal defects, and arrhythmias, such as ectopic atrial tachycardia, have been reported in a small proportion of patients with NAA15‐related syndrome. Given the relationship between NAA10 and NAA15, we propose that HCM is also likely to occur in NAA15‐related disorder. We present two patients with pediatric HCM found to have NAA15‐related disorder via exome sequencing, providing the first evidence that variants in NAA15 can cause HCM.
- Is Part Of:
- American journal of medical genetics. Volume 185:Issue 1(2021)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 185:Issue 1(2021)
- Issue Display:
- Volume 185, Issue 1 (2021)
- Year:
- 2021
- Volume:
- 185
- Issue:
- 1
- Issue Sort Value:
- 2021-0185-0001-0000
- Page Start:
- 228
- Page End:
- 233
- Publication Date:
- 2020-10-26
- Subjects:
- exome sequencing -- hypertrophic cardiomyopathy -- NAA10 -- NAA15 -- neurodevelopmental disorder
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.61928 ↗
- 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:
- 15334.xml