Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study

被引:5
作者
Di Pisa, Veronica [1 ]
Provini, Federica [2 ,3 ]
Ubertiello, Sara [1 ]
Bonetti, Silvia [1 ]
Ricci, Emilia [1 ]
Ivanovski, Ivan [4 ,5 ]
Caraffi, Stefano Giuseppe [4 ]
Giordano, Lucio [6 ]
Accorsi, Patrizia [6 ]
Savasta, Salvatore [7 ]
Raviglione, Federico [8 ]
Boni, Antonella [9 ]
Grioni, Daniele [10 ]
Graziano, Claudio [11 ]
Garavelli, Livia [4 ]
Cordelli, Duccio Maria [1 ]
机构
[1] Univ Bologna, Child Neurol & Psychiat Unit, Dept Med & Surg Sci DIMEC, S Orsola Hosp, Bologna, Italy
[2] Univ Bologna, Dept Biomed & NeuroMotor Sci DiBiNeM, Bologna, Italy
[3] IRCCS Ist Sci Neurol Bologna, Bologna, Italy
[4] IRCCS Reggio Emilia, Azienda USL, Mother & Child Hlth Dept, Med Genet Unit, Reggio Emilia, Italy
[5] Univ Modena & Reggio Emilia, Dept Surg Med Dent & Morphol Sci Interest Transpl, Modena, Italy
[6] Spedale Civili, Neuropsychiat Dept, Brescia, Italy
[7] IRCCS San Matteo, Dept Pediat, Pavia, Italy
[8] UONPLA ASST Rhodense, H Child Neuropsychiat Unit, Milan, Italy
[9] IRCCS, Inst Neurol Sci Bologna, Child Neurol Unit, Bologna, Italy
[10] San Gerardo Hosp, Child Neurophysiol Unit, Monza, Italy
[11] Univ Bologna, S Orsola Hosp Bologna, Med Genet, Bologna, Italy
关键词
Mowat-wilson syndrome; Video-polysomnography; ESES; Sleep disturbances; ELECTRICAL STATUS EPILEPTICUS; ZFHX1B SIP1; CHILDREN; DISTURBANCE;
D O I
10.1016/j.sleep.2019.04.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Sleep disturbances are frequently reported in Mowat-Wilson Syndrome (MWS). The current study aimed to evaluate clinical and video-polysomnographic (VPSG) characteristics of the sleep architecture and abnormal electroencephalogram (EEG) patterns during sleep in MWS. Methods: Sixteen individuals with MWS (range 16 months-25 years), attending the Department of Child Neurology and Psychiatry of the University of Bologna, were included. The "Sleep Disturbances Scale for Children (SDSC)" questionnaire was administered to all parents of MWS patients, and all patients underwent a VPSG recording. Results: The analysis of the SDSC questionnaire revealed disturbances mainly at the sleep-wake transition and in initiating and maintaining sleep. Evaluation of sleep structure in MWS patients showed a significant reduction of total sleep time, an increase of wake after sleep onset and arousal index as compared to normal controls. An EEG pattern characterized by slowing of background activity and poverty of physiological sleep characterisitcs was observed in all patients. Moreover, in patients aged >7 years, anteriorly predominant spike and waves were observed, markedly activated by sleep configuring a sub-continuous or continuous activity. Conclusion: Our data (both clinical and VPSG) documented the presence of significant and clinically relevant sleep disturbances in MWS patients. Moreover, we identified a characteristic age-dependent sleep EEG pattern that could provide a new element to assist in the management of MWS. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 51
页数:8
相关论文
共 17 条
  • [1] Sleep phenotypes in infants and toddlers with neurogenetic syndromes
    Abel, Emily A.
    Tonnsen, Bridgette L.
    [J]. SLEEP MEDICINE, 2017, 38 : 130 - 134
  • [2] Adam MP., 2007, GeneReviews, P1993
  • [3] Sleep in Children with Neurodevelopmental Disabilities
    Angriman, Marco
    Caravale, Barbara
    Novelli, Luana
    Ferri, Raffaele
    Bruni, Oliviero
    [J]. NEUROPEDIATRICS, 2015, 46 (03) : 199 - 210
  • [4] [Anonymous], 2014, AASM MANUAL SCORING
  • [5] Electrical status epilepticus during sleep in Mowat-Wilson syndrome
    Bonanni, Paolo
    Negrin, Susanna
    Volzone, Anna
    Zanotta, Nicoletta
    Epifanio, Roberta
    Zucca, Claudio
    Osanni, Elisa
    Petacchi, Elisa
    Fabbro, Franco
    [J]. BRAIN & DEVELOPMENT, 2017, 39 (09) : 727 - 734
  • [6] The sleep disturbance scale for children (SDSC) construction and validation of an instrument to evaluate sleep disturbances in childhood and adolescence
    Bruni, O
    Ottaviano, S
    Guidetti, V
    Romoli, M
    Innocenzi, M
    Cortesi, F
    Giannotti, F
    [J]. JOURNAL OF SLEEP RESEARCH, 1996, 5 (04) : 251 - 261
  • [7] Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype
    Cordelli, Duccio Maria
    Garavelli, Livia
    Savasta, Salvatore
    Guerra, Azzurra
    Pellicciari, Alessandro
    Giordano, Lucio
    Bonetti, Silvia
    Cecconi, Ilaria
    Wischmeijer, Anita
    Seri, Marco
    Rosato, Simonetta
    Gelmini, Chiara
    Della Giustina, Elvio
    Ferrari, Anna Rita
    Zanotta, Nicoletta
    Epifanio, Roberta
    Grioni, Daniele
    Malbora, Baris
    Mammi, Isabella
    Mari, Francesca
    Buoni, Sabrina
    Mostardini, Rosa
    Grosso, Salvatore
    Pantaleoni, Chiara
    Doz, Morena
    Luisa Poch-Olive, Maria
    Rivieri, Francesca
    Sorge, Giovanni
    Simonte, Graziella
    Licata, Francesca
    Tarani, Luigi
    Terazzi, Emanuela
    Mazzanti, Laura
    Mainardi, Paola Cerruti
    Boni, Antonella
    Faravelli, Francesca
    Grasso, Marina
    Bianchi, Paolo
    Zollino, Marcella
    Franzoni, Emilio
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (02) : 273 - 284
  • [8] Sleep Disturbance in Mowat-Wilson Syndrome
    Evans, Elizabeth
    Mowat, David
    Wilson, Meredith
    Einfeld, Stewart
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (03) : 654 - 660
  • [9] Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1):: Confirmation of the Mowat-Wilson syndrome
    Garavelli, L
    Donadio, A
    Zanacca, C
    Banchini, G
    Della Giustina, E
    Bertani, G
    Albertini, G
    Del Rossi, C
    Zweier, C
    Rauch, A
    Zollino, M
    Neri, G
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 116A (04) : 385 - 388
  • [10] Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients
    Garavelli, Livia
    Ivanovski, Ivan
    Caraffi, Stefano Giuseppe
    Santodirocco, Daniela
    Pollazzon, Marzia
    Cordelli, Duccio Maria
    Abdalla, Ebtesam
    Accorsi, Patrizia
    Adam, Margaret P.
    Baldo, Chiara
    Bayat, Allan
    Belligni, Elga
    Bonvicini, Federico
    Breckpot, Jeroen
    Callewaert, Bert
    Cocchi, Guido
    Cuturilo, Goran
    Devriendt, Koenraad
    Dinulos, Mary Beth
    Djuric, Olivera
    Epifanio, Roberta
    Faravelli, Francesca
    Formisano, Debora
    Giordano, Lucio
    Grasso, Marina
    Gronborg, Sabine
    Iodice, Alessandro
    Iughetti, Lorenzo
    Lacombe, Didier
    Maggi, Massimo
    Malbora, Baris
    Mammi, Isabella
    Moutton, Sebastien
    Moller, Rikke
    Muschke, Petra
    Napoli, Manuela
    Pantaleoni, Chiara
    Pascarella, Rosario
    Pellicciari, Alessandro
    Luisa Poch-Olive, Maria
    Raviglione, Federico
    Rivieri, Francesca
    Russo, Carmela
    Savasta, Salvatore
    Scarano, Gioacchino
    Selicorni, Angelo
    Silengo, Margherita
    Sorge, Giovanni
    Tarani, Luigi
    Tone, Luis Gonzaga
    [J]. GENETICS IN MEDICINE, 2017, 19 (06) : 691 - 700