Literature DB >> 26768041

Management of the behavioural manifestations of Hunter syndrome.

Jane Roberts1, Catherine Stewart2, Shauna Kearney3.   

Abstract

This article reviews the behavioural manifestations of, and the strategies for managing, Hunter syndrome (mucopolysaccharidosis (MPS) type II), a rare X-linked lysosomal storage disorder caused by a deficiency of the enzyme iduronate-2-sulphatase. Hunter syndrome is generally considered to have two manifestations: an attenuated form and a severe form; in the latter, the person has pronounced cognitive decline. Infants with either phenotype usually appear normal at birth, but may show some somatic signs. Children with the severe phenotype show developmental delay and changes in behaviour patterns at about 18 months to 4 years of age. To varying degrees, patients with the severe form manifest behavioural disorders such as hyperactivity, aggression, impulsivity, anxiety and sleep disturbances. Medications, such as antipsychotics, benzodiazepines and anticonvulsants, have been tried with varying degrees of success. Behavioural management strategies may be a worthwhile approach, although published data are lacking. For sleep disturbances, behavioural modification plus melatonin or benzodiazepine may be effective treatments.

Entities:  

Keywords:  Behavioural problems; Hunter syndrome; Lysosomal storage disorder; Mucopolysaccharidosis (MPS) type II

Mesh:

Substances:

Year:  2016        PMID: 26768041     DOI: 10.12968/bjon.2016.25.1.22

Source DB:  PubMed          Journal:  Br J Nurs        ISSN: 0966-0461


  9 in total

1.  A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report.

Authors:  Caio Perez Gomes; Maryana Mara Marins; Fabiana Louise Motta; Sandra Obikawa Kyosen; Marco Antonio Curiati; Vânia D'Almeida; Ana Maria Martins; João Bosco Pesquero
Journal:  Front Genet       Date:  2020-03-18       Impact factor: 4.599

2.  Response to: Investigating the neurobehavioral symptoms of neuronopathic Hunter syndrome.

Authors:  J B Eisengart; K E King; E Shapiro; C B Whitley; J Muenzer
Journal:  Mol Genet Metab Rep       Date:  2020-02-04

3.  Evaluating strategies to manage and endure challenging behaviors in mucopolysaccharidoses.

Authors:  Nathan Grant
Journal:  Orphanet J Rare Dis       Date:  2021-04-08       Impact factor: 4.123

4.  Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair.

Authors:  Nathan Grant; Young Bae Sohn; N Matthew Ellinwood; Ericka Okenfuss; Bryce A Mendelsohn; Leslie E Lynch; Elizabeth A Braunlin; Paul R Harmatz; Julie B Eisengart
Journal:  Mol Genet Metab Rep       Date:  2022-02-02

5.  Detailed pedigree analyses and prenatal diagnosis for a family with mucopolysaccharidosis type II.

Authors:  Chuan Zhang; Shengju Hao; ZhaoYan Meng; Ling Hui; Yan Wang; Feng Xuan; Xue Chen; Xing Wang; Furong Zheng; Lei Zheng; Bingbo Zhou; Xinqi Wu; Qinghua Zhang; Zongfu Cao
Journal:  BMC Med Genomics       Date:  2021-06-30       Impact factor: 3.063

6.  Brain RNA-Seq Profiling of the Mucopolysaccharidosis Type II Mouse Model.

Authors:  Marika Salvalaio; Francesca D'Avanzo; Laura Rigon; Alessandra Zanetti; Michela D'Angelo; Giorgio Valle; Maurizio Scarpa; Rosella Tomanin
Journal:  Int J Mol Sci       Date:  2017-05-17       Impact factor: 5.923

7.  Investigating the neurobehavioral symptoms of neuronopathic Hunter syndrome.

Authors:  Nathan Grant
Journal:  Mol Genet Metab Rep       Date:  2020-01-16

8.  The nature and impact of neurobehavioral symptoms in neuronopathic Hunter syndrome.

Authors:  J B Eisengart; K E King; E G Shapiro; C B Whitley; J Muenzer
Journal:  Mol Genet Metab Rep       Date:  2019-12-20

Review 9.  Challenging behavior in mucopolysaccharidoses types I-III and day-to-day coping strategies: a cross sectional explorative study.

Authors:  Frederik Hoffmann; Susanne Hoffmann; Kevin Kunzmann; Markus Ries
Journal:  Orphanet J Rare Dis       Date:  2020-10-02       Impact factor: 4.123

  9 in total

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