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Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association
Billion of years ago bacteria is believed to have entered a eukaryotic cell and converted to mitochondria. The respiratory chain present in it supplies ATP to all cells and therefore the diseases can have any phenotype. Diagnosis may be difficult to confirm by the conventional methods including gene...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227760/ https://www.ncbi.nlm.nih.gov/pubmed/32435307 http://dx.doi.org/10.4103/JPN.JPN_94_19 |
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author | Chandra, Sadanandavalli Retnaswami Padmanabha, Hansashree Gupta, Manisha Pruthi, Nupur Narayanappa, Gayathri Christopher, Rita |
author_facet | Chandra, Sadanandavalli Retnaswami Padmanabha, Hansashree Gupta, Manisha Pruthi, Nupur Narayanappa, Gayathri Christopher, Rita |
author_sort | Chandra, Sadanandavalli Retnaswami |
collection | PubMed |
description | Billion of years ago bacteria is believed to have entered a eukaryotic cell and converted to mitochondria. The respiratory chain present in it supplies ATP to all cells and therefore the diseases can have any phenotype. Diagnosis may be difficult to confirm by the conventional methods including genetics. Two brothers born to consanguineous parents had global delay, mild visual impairment and drooping of eyelids since birth in the elder child and dysmorphism in the second one. Both had progressive myelopathy due to retroflexed odontoid ,large arachnoid cyst and tethered cord. Muscle biopsy with special stain was normal but respiratory chain assay revealed severe complex 1 deficiency.Elder child underwent surgical decompression of the arachnoid cyst with duroplasty with significant improvement.Atlanto axial dislocation and large arachnoid cyst as cause of myelopathy is not reported in literature in patients with respiratory chain disorders to the best of our knowledge. |
format | Online Article Text |
id | pubmed-7227760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-72277602020-05-20 Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association Chandra, Sadanandavalli Retnaswami Padmanabha, Hansashree Gupta, Manisha Pruthi, Nupur Narayanappa, Gayathri Christopher, Rita J Pediatr Neurosci Case Report Billion of years ago bacteria is believed to have entered a eukaryotic cell and converted to mitochondria. The respiratory chain present in it supplies ATP to all cells and therefore the diseases can have any phenotype. Diagnosis may be difficult to confirm by the conventional methods including genetics. Two brothers born to consanguineous parents had global delay, mild visual impairment and drooping of eyelids since birth in the elder child and dysmorphism in the second one. Both had progressive myelopathy due to retroflexed odontoid ,large arachnoid cyst and tethered cord. Muscle biopsy with special stain was normal but respiratory chain assay revealed severe complex 1 deficiency.Elder child underwent surgical decompression of the arachnoid cyst with duroplasty with significant improvement.Atlanto axial dislocation and large arachnoid cyst as cause of myelopathy is not reported in literature in patients with respiratory chain disorders to the best of our knowledge. Wolters Kluwer - Medknow 2020 2020-03-18 /pmc/articles/PMC7227760/ /pubmed/32435307 http://dx.doi.org/10.4103/JPN.JPN_94_19 Text en Copyright: © 2020 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Chandra, Sadanandavalli Retnaswami Padmanabha, Hansashree Gupta, Manisha Pruthi, Nupur Narayanappa, Gayathri Christopher, Rita Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title | Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title_full | Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title_fullStr | Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title_full_unstemmed | Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title_short | Myelopathy in Two Brothers with Respiratory Chain Disorder–Severe Complex 1 Deficiency with Atlantoaxial Dislocation and Long Spinal Arachnoid Cyst: A New Unreported Association |
title_sort | myelopathy in two brothers with respiratory chain disorder–severe complex 1 deficiency with atlantoaxial dislocation and long spinal arachnoid cyst: a new unreported association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227760/ https://www.ncbi.nlm.nih.gov/pubmed/32435307 http://dx.doi.org/10.4103/JPN.JPN_94_19 |
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