Literature DB >> 32173091

Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation.

Müge Ayanoğlu1, Elif Korgali2, Taner Sezer3, Halil Ibrahim Aydin4, Fatma Müjgan Sönmez5.   

Abstract

We describe the first child with guanidinoacetate methyltransferase (GAMT) deficiency who developed neuroleptic malignant syndrome (NMS) after the treatment of risperidone without elevated creatine kinase (CK) levels. The patient presented with lethargy, hyperthermia, generalized tremor and rigidity with normal serum CK levels. After cessation of risperidone and adding clonezepam to the supportive treatment, symptoms of NMS were ameliorated. We conclude that although serum CK elevation is a useful indicator for the early detection of NMS, normal serum CK levels may be seen during the NMS course in the presence of GAMT deficiency.
Copyright © 2020 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

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Keywords:  Guanidinoacetate methyltransferase (GAMT) deficiency; Neuroleptic malignant syndrome; Normal creatine kinase levels

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Year:  2020        PMID: 32173091     DOI: 10.1016/j.braindev.2020.02.001

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  1 in total

Review 1.  Intellectual Disability and Brain Creatine Deficit: Phenotyping of the Genetic Mouse Model for GAMT Deficiency.

Authors:  Luigia Rossi; Francesca Nardecchia; Francesca Pierigè; Rossella Ventura; Claudia Carducci; Vincenzo Leuzzi; Mauro Magnani; Simona Cabib; Tiziana Pascucci
Journal:  Genes (Basel)       Date:  2021-08-02       Impact factor: 4.096

  1 in total

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