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.

Bibliographic Details
Main Authors: Sevria Yetty Anggraina Noer, Sunartini Sunartini, Purnomo Suryantoro
Format: Article
Language:English
Published: Indonesian Pediatric Society Publishing House 2022-07-01
Series:Paediatrica Indonesiana
Subjects:
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.
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2338-476X
language English
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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