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Neurogenic Bladder: A Rare Autonomic Sign in a Patient With Preserved Speech Variant (Zappella Variant) Rett Syndrome

Year 2024, , 256 - 259, 22.07.2024
https://doi.org/10.12956/tchd.1408162

Abstract

Background: Rett syndrome is characterized by the loss of speech and purposeful hand movements, ambulation problems, and typical hand stereotypies. Preserved speech variant Rett syndrome (Zappella Variant) is a much less common form where speech is relatively preserved, from words to simple sentences. Lower urinary tract dysfunction and neurogenic bladder due to autonomic involvement have been only rarely reported in Rett syndrome. We aimed to emphasize neurogenic bladder due to autonomic dysfunction, which has very rarely been reported in the literature, in a patient with preserved speech variant Rett syndrome, a rare form of the Rett syndrome.

Case presentation: A 7-year-old female patient who had been diagnosed with severe vesicoureteral reflux and neurogenic bladder when 11 months old due to the inability to urinate was suspected of suffering from Rett syndrome after intense eye contact and the stereotypic movement of hand wringing were observed. The patient could talk with phrases and walk and had purposeful hand movements. The presence of the c.961C>T (p.Arg321Trp) mutation in the C terminal region of the MECP2 gene was demonstrated with Sanger sequencing. The patient is currently 13 years old and is receiving special education and continues to be monitored for chronic renal disease at the pediatric nephrology department.

Conclusion: The presence of hand stereotypies and intense eye pointing could indicate the Zappella variant Rett syndrome in a female patient who has developmental problems, can talk, has purposeful hand skills. Rett syndrome patients can also have lower urinary tract dysfunction although this is less common than cardiac, respiratory and gastrointestinal autonomic involvement. The development of intermittent urinary retention and vesicoureteral reflux may be associated with neurogenic bladder caused by autonomic involvement should be considered in these patients and one must be aware of the complications.

References

  • Percy AK, Neul JL, Glaze DG, Motil KJ, Skinner SA, Khwaja O, et al. Rett syndrome diagnostic criteria: Lessons from the Natural History Study. Ann Neurol 2010; 68: 944–50.
  • Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, et al. Consensus guidelines on managing Rett syndrome across the lifespan. BMJ Paediatr Open 2020;4: e000717.
  • Frullanti E, Papa FT, Grillo E, Clarke A, Ben-Zeev B, Pineda M, et al. Analysis of the Phenotypes in the Rett Networked Database. Int J Genomics 2019; 6956934.
  • Renieri A, Mari F, Mencarelli MA, Scala E, Ariani F, Longo I, et al. Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant). Brain Dev 2009; 31: 208–216.
  • Leonard H, Cobb S, Downs J. Clinical and biological progress over 50 years in Rett syndrome. Nat Rev Neurol 2017; 13:37-51.
  • Ivy AS, Standridge SM. Rett Syndrome: A timely review from recognition to current clinical approaches and clinical study updates. Semin Pediatr Neurol 2021;37:100881.
  • Singh J, Santosh P. Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD)- a target for clinical trials. Orphanet J Rare Dis 2018;13:128.
  • Halbach N, Smeets EE, Julu P, Witt-Engerström I, Pini G, Bigoni S et al. Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. Am J Med Genet A 2016;170:2301-9.
  • Pini G, Bigoni S, Congiu L, Romanelli AM, Scusa MF, Di Marco P, et al. Rett syndrome: a wide clinical and autonomic picture. Orphanet J Rare Dis 2016;11:132.
  • Lioy DT, Wu WW, Bissonnette JM. Autonomic dysfunction with mutations in the gene that encodes methyl-CpG-binding protein 2: Insights into Rett syndrome. Auton Neurosci 2011;161:55-62.
  • Marschik PB, Pini G, Bartl-Pokorny KD, Duckworth M, Gugatschka M, Vollmann R, et al. Early speech-language development in females with Rett syndrome: focusing on the preserved speech variant. Dev Med Child Neurol 2012; 54:451-6.
  • Doelman AW, Streijger F, Majerus SJA, Damaser MS, Kwon BK. Assessing neurogenic lower urinary tract dysfunction after spinal cord injury:Animal models in preclinical neuro-urology research. Biomedicines 2023;11:1539.
  • Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, et al. Loss of MECP2 causes urological dysfunction and contributes to death by kidney failure in mouse models of Rett syndrome. PLoS One 2016;11: e0165550.
  • Roth JD, Pariser JJ, Stout TE, Misseri R, Elliot SP. Presentation and management patterns of lower urinary tract symptoms in adults due to rare inherited neuromuscular diseases. Urology 2020;135:165-70.
  • Park HE, Lee JS, Kim DM, Shin YB. Two pediatric cases of successful management of postictal transient urinary retention. Ann Rehabil Med 2020;44:90-93.
  • Li W, Pozzo-Miller L. BDNF deregulation in Rett syndrome. Neuropharmacology 2014; 76:737-46.
  • Frias B, Allen S, Dawbarn D, Charrua A, Cruz F, Cruz CD. Brain derived neurotrophic factor, acting at the spinal cord level, participates in bladder hyperactivity and referred pain during chronic bladder inflammation. Neuroscience 2013; 234:88-102.

Nörojenik Mesane: Rett Sendromunun Korunmuş Konuşma Varyantı (Zappella Varyantı) Olan Hastada Nadir Bir Otonom Belirti

Year 2024, , 256 - 259, 22.07.2024
https://doi.org/10.12956/tchd.1408162

Abstract

Giriş-Amaç: Rett sendromu, konuşma ve anlamlı el hareketlerinin kaybı, yürüme sorunları ve tipik el stereotipleri ile karakterizedir. Konuşmanın korunduğu varyantı Rett sendromu (Zappella Variant), kelimelerden basit cümlelere kadar konuşmanın nispeten korunduğu daha az yaygın bir formdur. Rett sendromunda alt üriner sistem disfonksiyonu ve otonomik tutuluma bağlı nörojenik mesane nadiren rapor edilmiştir. Rett sendromunun nadir görülen bir formu olan korunmuş konuşma varyantı Rett sendromu olan bir hastada, literatürde çok nadir bildirilen otonomik disfonksiyona bağlı nörojenik mesaneyi vurgulamayı amaçladık.

Vaka sunumu: İdrar yapamama nedeniyle 11 aylıkken şiddetli vezikoüreteral reflü ve nörojenik mesane tanısı konulan 7 yaşındaki kız hastanın, yoğun göz teması ve basmakalıp el ovuşturma hareketi sonrasında Rett sendromundan şüphelenildi. Hasta cümlelerle konuşabiliyor, yürüyebiliyor ve amaçlı el hareketleri yapabiliyordu. MECP2 geninin C terminal bölgesinde c.961C>T (p.Arg321Trp) mutasyonunun varlığı sanger dizilimi ile gösterildi. Hasta şu anda 13 yaşında özel eğitim almakta olup, çocuk nefrolojisi bölümünde kronik böbrek hastalığı açısından takip edilmeye devam etmektedir.

Sonuç: Gelişimsel sorunları olan, konuşabilen, amaçlı el becerilerine sahip bir kadın hastada sterotipik el hareketleri ve yoğun göz teması varlığı Zappella varyantı Rett sendromuna işaret edebilir. Rett sendromu hastalarında ayrıca alt üriner sistem disfonksiyonu da görülebilir, ancak bu durum kalp, solunum ve gastrointestinal otonomik tutulumdan daha az görülür. Bu hastalarda intermittan idrar retansiyonu ve vezikoüreteral reflü gelişiminin otonomik tutuluma bağlı nörojenik mesane ile ilişkili olabileceği göz önünde bulundurulmalı ve komplikasyonlara karşı dikkatli olunmalıdır.

References

  • Percy AK, Neul JL, Glaze DG, Motil KJ, Skinner SA, Khwaja O, et al. Rett syndrome diagnostic criteria: Lessons from the Natural History Study. Ann Neurol 2010; 68: 944–50.
  • Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, et al. Consensus guidelines on managing Rett syndrome across the lifespan. BMJ Paediatr Open 2020;4: e000717.
  • Frullanti E, Papa FT, Grillo E, Clarke A, Ben-Zeev B, Pineda M, et al. Analysis of the Phenotypes in the Rett Networked Database. Int J Genomics 2019; 6956934.
  • Renieri A, Mari F, Mencarelli MA, Scala E, Ariani F, Longo I, et al. Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant). Brain Dev 2009; 31: 208–216.
  • Leonard H, Cobb S, Downs J. Clinical and biological progress over 50 years in Rett syndrome. Nat Rev Neurol 2017; 13:37-51.
  • Ivy AS, Standridge SM. Rett Syndrome: A timely review from recognition to current clinical approaches and clinical study updates. Semin Pediatr Neurol 2021;37:100881.
  • Singh J, Santosh P. Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD)- a target for clinical trials. Orphanet J Rare Dis 2018;13:128.
  • Halbach N, Smeets EE, Julu P, Witt-Engerström I, Pini G, Bigoni S et al. Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. Am J Med Genet A 2016;170:2301-9.
  • Pini G, Bigoni S, Congiu L, Romanelli AM, Scusa MF, Di Marco P, et al. Rett syndrome: a wide clinical and autonomic picture. Orphanet J Rare Dis 2016;11:132.
  • Lioy DT, Wu WW, Bissonnette JM. Autonomic dysfunction with mutations in the gene that encodes methyl-CpG-binding protein 2: Insights into Rett syndrome. Auton Neurosci 2011;161:55-62.
  • Marschik PB, Pini G, Bartl-Pokorny KD, Duckworth M, Gugatschka M, Vollmann R, et al. Early speech-language development in females with Rett syndrome: focusing on the preserved speech variant. Dev Med Child Neurol 2012; 54:451-6.
  • Doelman AW, Streijger F, Majerus SJA, Damaser MS, Kwon BK. Assessing neurogenic lower urinary tract dysfunction after spinal cord injury:Animal models in preclinical neuro-urology research. Biomedicines 2023;11:1539.
  • Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, et al. Loss of MECP2 causes urological dysfunction and contributes to death by kidney failure in mouse models of Rett syndrome. PLoS One 2016;11: e0165550.
  • Roth JD, Pariser JJ, Stout TE, Misseri R, Elliot SP. Presentation and management patterns of lower urinary tract symptoms in adults due to rare inherited neuromuscular diseases. Urology 2020;135:165-70.
  • Park HE, Lee JS, Kim DM, Shin YB. Two pediatric cases of successful management of postictal transient urinary retention. Ann Rehabil Med 2020;44:90-93.
  • Li W, Pozzo-Miller L. BDNF deregulation in Rett syndrome. Neuropharmacology 2014; 76:737-46.
  • Frias B, Allen S, Dawbarn D, Charrua A, Cruz F, Cruz CD. Brain derived neurotrophic factor, acting at the spinal cord level, participates in bladder hyperactivity and referred pain during chronic bladder inflammation. Neuroscience 2013; 234:88-102.
There are 17 citations in total.

Details

Primary Language English
Subjects Clinical Sciences (Other)
Journal Section CASE REPORTS
Authors

Özge Tanıdır Artan 0000-0002-9773-5497

Büşranur Çavdarlı 0000-0002-0953-6210

Umut Selda Bayrakçı 0000-0002-5301-2617

Bilge Karabulut 0000-0002-5113-7467

Aydan Değerliyurt 0000-0001-9776-9390

Early Pub Date May 20, 2024
Publication Date July 22, 2024
Submission Date December 21, 2023
Acceptance Date April 2, 2024
Published in Issue Year 2024

Cite

Vancouver Tanıdır Artan Ö, Çavdarlı B, Bayrakçı US, Karabulut B, Değerliyurt A. Neurogenic Bladder: A Rare Autonomic Sign in a Patient With Preserved Speech Variant (Zappella Variant) Rett Syndrome. Türkiye Çocuk Hast Derg. 2024;18(4):256-9.

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