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Mirror movement associated with neural tube defects

OBJECTIVE: Association of mirror movements with special kinds of neural tube defects, particularly cranial dermal sinus and cervical myelomeningocele, is extremely rare. We have tried to explain the probable pathophysiology underlying this rare condition. CLINICAL PRESENTATION: Two cases are present...

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Autores principales: Andrabi, Yasir, Nejat, Farideh, Khashab, Mostafa El, Ashrafi, Mohammad Reza
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646657/
https://www.ncbi.nlm.nih.gov/pubmed/19337468
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author Andrabi, Yasir
Nejat, Farideh
Khashab, Mostafa El
Ashrafi, Mohammad Reza
author_facet Andrabi, Yasir
Nejat, Farideh
Khashab, Mostafa El
Ashrafi, Mohammad Reza
author_sort Andrabi, Yasir
collection PubMed
description OBJECTIVE: Association of mirror movements with special kinds of neural tube defects, particularly cranial dermal sinus and cervical myelomeningocele, is extremely rare. We have tried to explain the probable pathophysiology underlying this rare condition. CLINICAL PRESENTATION: Two cases are presented. Case 1: A right-handed 3-year-old boy brought to the outpatient clinic for evaluation of mirror movement had been operated on at 10 days of age to repair a cervical myelomeningocele. At examination, mirror movements were observed on both sides. Case 2: A right-handed 7-year-old boy referred for vertigo and occasional vomiting since 3 months of age. The mirror movements were present in the upper extremities, and reportedly had existed since early childhood. Brain magnetic resonance imaging disclosed the dermal sinus, tract, and midline dermoid tumor. CONCLUSION: To describe a meaningful association between mirror movements and congenital abnormalities in 2 cases reported here, we propose development of an abnormality in the cervical spinal cord (case 1) and cervicomedullary junction (case 2) associated with gross anomalies in the affected areas.
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spelling pubmed-26466572009-04-01 Mirror movement associated with neural tube defects Andrabi, Yasir Nejat, Farideh Khashab, Mostafa El Ashrafi, Mohammad Reza Neuropsychiatr Dis Treat Case Report OBJECTIVE: Association of mirror movements with special kinds of neural tube defects, particularly cranial dermal sinus and cervical myelomeningocele, is extremely rare. We have tried to explain the probable pathophysiology underlying this rare condition. CLINICAL PRESENTATION: Two cases are presented. Case 1: A right-handed 3-year-old boy brought to the outpatient clinic for evaluation of mirror movement had been operated on at 10 days of age to repair a cervical myelomeningocele. At examination, mirror movements were observed on both sides. Case 2: A right-handed 7-year-old boy referred for vertigo and occasional vomiting since 3 months of age. The mirror movements were present in the upper extremities, and reportedly had existed since early childhood. Brain magnetic resonance imaging disclosed the dermal sinus, tract, and midline dermoid tumor. CONCLUSION: To describe a meaningful association between mirror movements and congenital abnormalities in 2 cases reported here, we propose development of an abnormality in the cervical spinal cord (case 1) and cervicomedullary junction (case 2) associated with gross anomalies in the affected areas. Dove Medical Press 2008-12 /pmc/articles/PMC2646657/ /pubmed/19337468 Text en © 2008 Dove Medical Press Limited. All rights reserved
spellingShingle Case Report
Andrabi, Yasir
Nejat, Farideh
Khashab, Mostafa El
Ashrafi, Mohammad Reza
Mirror movement associated with neural tube defects
title Mirror movement associated with neural tube defects
title_full Mirror movement associated with neural tube defects
title_fullStr Mirror movement associated with neural tube defects
title_full_unstemmed Mirror movement associated with neural tube defects
title_short Mirror movement associated with neural tube defects
title_sort mirror movement associated with neural tube defects
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646657/
https://www.ncbi.nlm.nih.gov/pubmed/19337468
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