Neuropediatrics 2018; 49(05): 339-341
DOI: 10.1055/s-0038-1667024
Short Communication
Georg Thieme Verlag KG Stuttgart · New York

Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review

Authors

  • Thouraya Ben Younes

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
  • Hanene Benrhouma

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
  • Hedia Klaa

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
  • Aida Rouissi

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
  • Myriam Chaabouni

    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
    3   Laboratory of Medical Analyzes and Human Genetics, Jasmins Medical Center, Tunis, Tunisia
  • Ichraf Kraoua

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
  • Ilhem Ben Youssef-Turki

    1   Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    2   Université de Tunis El Manar, Faculté de Médecine de Tunis, Tunis, Tunisia
Further Information

Publication History

26 February 2018

04 June 2018

Publication Date:
16 July 2018 (online)

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Abstract

ATP1A3 mutations have now been recognized in infants, children, and adults presenting with a diverse group of neurological phenotypes, including rapid-onset dystonia-parkinsonism, alternating hemiplegia of childhood, and most recently, cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss syndrome. The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand. In this case study, we report on early life epilepsy with episodic apnea potentially secondary to ATP1A3 mutation in a Tunisian child.