Literature DB >> 11030068

Delayed diagnosis of Duchenne muscular dystrophy.

K Mohamed1, R Appleton, P Nicolaides.   

Abstract

A late diagnosis of Duchenne muscular dystrophy has implications for both child and family. This repeat audit has shown that the diagnosis continues to be delayed. The failure to recognize that non-motor, and specifically speech and language delay are common features of this disease may detract from the motor difficulties in affected children and contribute to the late diagnosis of this disorder. In the absence of a national newborn screening programme for Duchenne muscular dystrophy, all health care professionals should be made more aware of the condition and have a lower threshold for measuring a creatine phosphokinase level.

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Year:  2000        PMID: 11030068     DOI: 10.1053/ejpn.2000.0309

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  17 in total

Review 1.  Cerebral palsy: not always what it seems.

Authors:  R Gupta; R E Appleton
Journal:  Arch Dis Child       Date:  2001-11       Impact factor: 3.791

Review 2.  Should creatine kinase be checked in all boys presenting with speech delay?

Authors:  Claire T Lundy; Gary M Doherty; Elaine M Hicks
Journal:  Arch Dis Child       Date:  2007-07       Impact factor: 3.791

Review 3.  Clinical management of Duchenne muscular dystrophy: the state of the art.

Authors:  Sonia Messina; Gian Luca Vita
Journal:  Neurol Sci       Date:  2018-09-14       Impact factor: 3.307

4.  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

5.  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

6.  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

7.  Delayed developmental language milestones in children with Duchenne's muscular dystrophy.

Authors:  Shana E Cyrulnik; Robert J Fee; Darryl C De Vivo; Edward Goldstein; Veronica J Hinton
Journal:  J Pediatr       Date:  2007-05       Impact factor: 4.406

8.  Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK).

Authors:  Stuart J Moat; Donald M Bradley; Rachel Salmon; Angus Clarke; Louise Hartley
Journal:  Eur J Hum Genet       Date:  2013-01-23       Impact factor: 4.246

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

Authors:  Emma Ciafaloni; 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
Journal:  J Pediatr       Date:  2009-04-25       Impact factor: 4.406

10.  Muscle histology vs MRI in Duchenne muscular dystrophy.

Authors:  M Kinali; V Arechavala-Gomeza; S Cirak; A Glover; M Guglieri; L Feng; K G Hollingsworth; D Hunt; H Jungbluth; H P Roper; R M Quinlivan; J A Gosalakkal; S Jayawant; A Nadeau; L Hughes-Carre; A Y Manzur; E Mercuri; J E Morgan; V Straub; K Bushby; C Sewry; M Rutherford; F Muntoni
Journal:  Neurology       Date:  2011-01-25       Impact factor: 9.910

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