Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case
Duchenne muscular dystrophy (DMD) is a X-linked recessive gene defect manifesting as a fatal, progressive neuromuscular disease. Treatment goals aim to inhibit disease progression, increase patients’ quality of life, and lengthen life expectancy. We report here a single case of non-ambulatory DMD.
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Format: | Article |
Language: | English |
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Indonesian Pediatric Society Publishing House
2022-07-01
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Series: | Paediatrica Indonesiana |
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Online Access: | https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2447 |
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author | Sevria Yetty Anggraina Noer Sunartini Sunartini Purnomo Suryantoro |
author_facet | Sevria Yetty Anggraina Noer Sunartini Sunartini Purnomo Suryantoro |
author_sort | Sevria Yetty Anggraina Noer |
collection | DOAJ |
description | Duchenne muscular dystrophy (DMD) is a X-linked recessive gene defect manifesting as a fatal, progressive neuromuscular disease. Treatment goals aim to inhibit disease progression, increase patients’ quality of life, and lengthen life expectancy. We report here a single case of non-ambulatory DMD. |
first_indexed | 2024-04-14T04:28:47Z |
format | Article |
id | doaj.art-b39503607d4d48ba837e00f015cf5609 |
institution | Directory Open Access Journal |
issn | 0030-9311 2338-476X |
language | English |
last_indexed | 2024-04-14T04:28:47Z |
publishDate | 2022-07-01 |
publisher | Indonesian Pediatric Society Publishing House |
record_format | Article |
series | Paediatrica Indonesiana |
spelling | doaj.art-b39503607d4d48ba837e00f015cf56092022-12-22T02:12:09ZengIndonesian Pediatric Society Publishing HousePaediatrica Indonesiana0030-93112338-476X2022-07-016232081610.14238/pi62.3.2022.208-162447Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single caseSevria Yetty Anggraina Noer0Sunartini Sunartini1Purnomo Suryantoro2Universitas Gadjah Mada - RSUP dr. SardjitoUniversitas Gadjah Mada - RSUP dr. SardjitoUniversitas Gadjah Mada - RSUP dr. SardjitoDuchenne muscular dystrophy (DMD) is a X-linked recessive gene defect manifesting as a fatal, progressive neuromuscular disease. Treatment goals aim to inhibit disease progression, increase patients’ quality of life, and lengthen life expectancy. We report here a single case of non-ambulatory DMD.https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2447duchenne muscular dystrophy; non-ambulatory; gene deletion; outcome |
spellingShingle | Sevria Yetty Anggraina Noer Sunartini Sunartini Purnomo Suryantoro Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case Paediatrica Indonesiana duchenne muscular dystrophy; non-ambulatory; gene deletion; outcome |
title | Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case |
title_full | Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case |
title_fullStr | Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case |
title_full_unstemmed | Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case |
title_short | Non-ambulatory Duchenne muscular dystrophy: observations, interventions, and outcomes on a single case |
title_sort | non ambulatory duchenne muscular dystrophy observations interventions and outcomes on a single case |
topic | duchenne muscular dystrophy; non-ambulatory; gene deletion; outcome |
url | https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2447 |
work_keys_str_mv | AT sevriayettyanggrainanoer nonambulatoryduchennemusculardystrophyobservationsinterventionsandoutcomesonasinglecase AT sunartinisunartini nonambulatoryduchennemusculardystrophyobservationsinterventionsandoutcomesonasinglecase AT purnomosuryantoro nonambulatoryduchennemusculardystrophyobservationsinterventionsandoutcomesonasinglecase |