Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: New insights into Brunner syndrome and potential for targeted therapy
Author: Palmer, E.
Leffler, M.
Rogers, C.
Shaw, M.
Carroll, R.
Earl, J.
Cheung, N.
Champion, B.
Hu, H.
Haas, S.
Kalscheuer, V.
Gecz, J.
Field, M.
Citation: Clinical Genetics: an international journal of genetics and molecular medicine, 2016; 89(1):120-127
Publisher: Wiley
Issue Date: 2016
ISSN: 0009-9163
Statement of
E.E. Palmer, M. Leffler, C. Rogers, M. Shaw, R. Carroll, J. Earl, N.W. Cheung, B. Champion, H. Hu, S.A. Haas, V.M. Kalscheuer, J. Gecz, and M. Field
Abstract: We report two families with Brunner syndrome living in one state of Australia. The first family had a predicted protein-truncating variant of monoamine oxidase A (MAOA) (p.S251KfsX2). Affected males had mild intellectual disability (ID), obsessive behaviour, limited friendships and were introverted and placid during clinical interview. The family disclosed episodic explosive aggression after a diagnosis was made. The second family had a missense variant in MAOA (p.R45W). Affected males had borderline-mild ID, attention deficit disorder and limited friendships. One had a history of explosive aggression in childhood and episodic symptoms of flushing, headaches and diarrhoea. Their carrier mother had normal intelligence but similar episodic symptoms. Characteristic biochemical abnormalities included high serum serotonin and urinary metanephrines and low urinary 5-hydroxyindoleacetic acid (5-HIAA) and vanillylmandelic acid (VMA). Symptomatic individuals in the second family had particularly high serotonin levels, and treatment with a serotonin reuptake inhibitor and dietary modification resulted in reversal of biochemical abnormalities, reduction of 'serotonergic' symptoms and behavioural improvement. Brunner syndrome should be considered as a cause of mild ID with paroxysmal behavioural symptoms. It can be screened for with serum/urine metanephrine and serotonin measurement. Cautious treatment with a serotonin reuptake inhibitor, dietary modifications and avoidance of medications contraindicated in patients on monoamine oxidase inhibitors can improve symptoms.
Keywords: Autism spectrum disorder; Brunner syndrome; diagnosis; intellectual disability; MAO-A deficiency; serotonin; treatment
Rights: © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
DOI: 10.1111/cge.12589
Grant ID:
Published version:
Appears in Collections:Aurora harvest 3
Paediatrics publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.