Literature DB >> 19394035

Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

Emma Ciafaloni1, Deborah J Fox, Shree Pandya, Christina P Westfield, Soman Puzhankara, Paul A Romitti, Katherine D Mathews, Timothy M Miller, Dennis J Matthews, Lisa A Miller, Christopher Cunniff, Charlotte M Druschel, Richard T Moxley.   

Abstract

OBJECTIVE: To identify key factors for the delay in diagnosis of Duchenne muscular dystrophy (DMD) without known family history. STUDY
DESIGN: The cohort comes from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet), a multistate, multiple-source, population-based surveillance system that identifies and gathers information on all cases of Duchenne and Becker muscular dystrophy born since 1982. We analyzed medical records of 453 Duchenne and Becker muscular dystrophy boys to document the time course and steps taken to reach a definitive diagnosis.
RESULTS: Among 156 boys without known family history of DMD prior to birth, first signs or symptoms were noted at a mean age of 2.5 years. Concerns resulted in primary care provider evaluation of the child at a mean age of 3.6 years. Mean age at time of initial creatine kinase was 4.7 years. Mean age at definitive diagnosis of DMD was 4.9 years.
CONCLUSIONS: There is a delay of about 2.5 years between onset of DMD symptoms and the time of definitive diagnosis, unchanged over the previous 2 decades. This delay results in lost opportunities for timely genetic counseling and initiation of corticosteroid treatment. We recommend checking creatine kinase early in the evaluation of boys with unexplained developmental delay.

Entities:  

Mesh:

Year:  2009        PMID: 19394035      PMCID: PMC5884059          DOI: 10.1016/j.jpeds.2009.02.007

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  23 in total

1.  A comparison of daily and alternate-day prednisone therapy in the treatment of Duchenne muscular dystrophy.

Authors:  G M Fenichel; J R Mendell; R T Moxley; R C Griggs; M H Brooke; J P Miller; A Pestronk; J Robison; W King; L Signore
Journal:  Arch Neurol       Date:  1991-06

Review 2.  Duchenne muscular dystrophy: issues in expanding newborn screening.

Authors:  Alex R Kemper; Melissa A Wake
Journal:  Curr Opin Pediatr       Date:  2007-12       Impact factor: 2.856

3.  Early diagnosis and secondary prevention of Duchenne muscular dystrophy.

Authors:  R A Smith; J R Sibert; S J Wallace; P S Harper
Journal:  Arch Dis Child       Date:  1989-06       Impact factor: 3.791

4.  Implications of diagnostic delay in Duchenne muscular dystrophy.

Authors:  T O'Brien; J R Sibert; P S Harper
Journal:  Br Med J (Clin Res Ed)       Date:  1983-10-15

5.  Diagnostic delay in Duchenne's muscular dystrophy.

Authors:  D E Crisp; F A Ziter; P F Bray
Journal:  JAMA       Date:  1982 Jan 22-29       Impact factor: 56.272

6.  The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology.

Authors:  Lisa A Miller; Paul A Romitti; Christopher Cunniff; Charlotte Druschel; Katherine D Mathews; F John Meaney; Dennis Matthews; Jiji Kantamneni; Zhen-Fang Feng; Nancy Zemblidge; Timothy M Miller; Jennifer Andrews; Deborah Fox; Emma Ciafaloni; Shree Pandya; April Montgomery; Aileen Kenneson
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2006-11

Review 7.  Delayed diagnosis of Duchenne muscular dystrophy.

Authors:  K Mohamed; R Appleton; P Nicolaides
Journal:  Eur J Paediatr Neurol       Date:  2000       Impact factor: 3.140

8.  Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.

Authors:  M Koenig; E P Hoffman; C J Bertelson; A P Monaco; C Feener; L M Kunkel
Journal:  Cell       Date:  1987-07-31       Impact factor: 41.582

9.  Diagnosis of Duchenne muscular dystrophy: parents' experiences and satisfaction.

Authors:  J M Green; F E Murton
Journal:  Child Care Health Dev       Date:  1996-03       Impact factor: 2.508

10.  Long-term benefit from prednisone therapy in Duchenne muscular dystrophy.

Authors:  G M Fenichel; J M Florence; A Pestronk; J R Mendell; R T Moxley; R C Griggs; M H Brooke; J P Miller; J Robison; W King
Journal:  Neurology       Date:  1991-12       Impact factor: 9.910

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  58 in total

1.  Patterns of decline in upper limb function of boys and men with DMD: an international survey.

Authors:  Mariska M H P Janssen; Arjen Bergsma; Alexander C H Geurts; Imelda J M de Groot
Journal:  J Neurol       Date:  2014-04-01       Impact factor: 4.849

2.  Diagnostic odyssey of patients with myotonic dystrophy.

Authors:  James E Hilbert; Tetsuo Ashizawa; John W Day; Elizabeth A Luebbe; William B Martens; Michael P McDermott; Rabi Tawil; Charles A Thornton; Richard T Moxley
Journal:  J Neurol       Date:  2013-06-27       Impact factor: 4.849

3.  Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.

Authors:  Elizabeth M McNally; Jonathan R Kaltman; D Woodrow Benson; Charles E Canter; Linda H Cripe; Dongsheng Duan; Jonathan D Finder; William J Groh; Eric P Hoffman; Daniel P Judge; Naomi Kertesz; Kathi Kinnett; Roxanne Kirsch; Joseph M Metzger; Gail D Pearson; Jill A Rafael-Fortney; Subha V Raman; Christopher F Spurney; Shari L Targum; Kathryn R Wagner; Larry W Markham
Journal:  Circulation       Date:  2015-05-05       Impact factor: 29.690

4.  Delayed onset of ambulation in boys with Duchenne muscular dystrophy: Potential use as an endpoint in clinical trials.

Authors:  Jacob J Gissy; Teresa Johnson; Deborah J Fox; Anil Kumar; Emma Ciafaloni; Anthonie J van Essen; Holly L Peay; Ann Martin; Ann Lucas; Richard S Finkel
Journal:  Neuromuscul Disord       Date:  2017-07-21       Impact factor: 4.296

5.  Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy.

Authors:  Sarah K Nabukera; Paul A Romitti; Kristin M Caspers; Natalie Street; Christopher Cunniff; Katherine D Mathews; Deborah J Fox; Soman Puzhankara; Emma Ciafaloni; Katherine A James; Yin Su
Journal:  Am J Med Genet A       Date:  2012-12-13       Impact factor: 2.802

6.  Parental Reflections on the Diagnostic Process for Duchenne Muscular Dystrophy: A Qualitative Study.

Authors:  Roxanna M Bendixen; Amy Houtrow
Journal:  J Pediatr Health Care       Date:  2016-10-12       Impact factor: 1.812

7.  Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data.

Authors:  Courtney R Carlson; Steven A Moore; Katherine D Mathews
Journal:  Muscle Nerve       Date:  2018-01-24       Impact factor: 3.217

8.  A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy.

Authors:  Siaw H Wong; Belinda J McClaren; Alison Dalton Archibald; Alice Weeks; Tess Langmaid; Monique M Ryan; Andrew Kornberg; Sylvia A Metcalfe
Journal:  Eur J Hum Genet       Date:  2015-01-28       Impact factor: 4.246

9.  Is There a Delay in Diagnosis of Duchenne Muscular Dystrophy Among Preterm-Born Males?

Authors:  Aida Soim; Michael G Smith; Jennifer M Kwon; Joshua R Mann; Shiny Thomas; Emma Ciafaloni
Journal:  J Child Neurol       Date:  2018-05-15       Impact factor: 1.987

10.  Nanotopography-responsive myotube alignment and orientation as a sensitive phenotypic biomarker for Duchenne Muscular Dystrophy.

Authors:  Bin Xu; Alessandro Magli; Yoska Anugrah; Steven J Koester; Rita C R Perlingeiro; Wei Shen
Journal:  Biomaterials       Date:  2018-08-21       Impact factor: 12.479

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