Cargando…
Cochlear implant and thiamine-responsive megaloblastic anemia syndrome
Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and bilateral sensorineural deafness, responding in varying degrees to thiamine treatment. We report a precedence case for the treatment of d...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074931/ https://www.ncbi.nlm.nih.gov/pubmed/24658560 http://dx.doi.org/10.5144/0256-4947.2014.78 |
_version_ | 1783344512556335104 |
---|---|
author | Hagr, Abdulrahman Abdullah |
author_facet | Hagr, Abdulrahman Abdullah |
author_sort | Hagr, Abdulrahman Abdullah |
collection | PubMed |
description | Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and bilateral sensorineural deafness, responding in varying degrees to thiamine treatment. We report a precedence case for the treatment of deafness associated with the typical triad of thiamine-responsive megaloblastic anemia in a 4-year-old boy who showed a poor use of preoperative hearing aids but demonstrated significant improvements in hearing ability 1 year after receiving a cochlear implant. |
format | Online Article Text |
id | pubmed-6074931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | King Faisal Specialist Hospital and Research Centre |
record_format | MEDLINE/PubMed |
spelling | pubmed-60749312018-09-21 Cochlear implant and thiamine-responsive megaloblastic anemia syndrome Hagr, Abdulrahman Abdullah Ann Saudi Med Case Report Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and bilateral sensorineural deafness, responding in varying degrees to thiamine treatment. We report a precedence case for the treatment of deafness associated with the typical triad of thiamine-responsive megaloblastic anemia in a 4-year-old boy who showed a poor use of preoperative hearing aids but demonstrated significant improvements in hearing ability 1 year after receiving a cochlear implant. King Faisal Specialist Hospital and Research Centre 2014 /pmc/articles/PMC6074931/ /pubmed/24658560 http://dx.doi.org/10.5144/0256-4947.2014.78 Text en Copyright © 2014, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Hagr, Abdulrahman Abdullah Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title | Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title_full | Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title_fullStr | Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title_full_unstemmed | Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title_short | Cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
title_sort | cochlear implant and thiamine-responsive megaloblastic anemia syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074931/ https://www.ncbi.nlm.nih.gov/pubmed/24658560 http://dx.doi.org/10.5144/0256-4947.2014.78 |
work_keys_str_mv | AT hagrabdulrahmanabdullah cochlearimplantandthiamineresponsivemegaloblasticanemiasyndrome |