Literature DB >> 3733820

Delay in diagnosing Duchenne muscular dystrophy in orthopaedic clinics.

L Read, C S Galasko.   

Abstract

For clinical, psychological and social reasons the diagnosis of Duchenne muscular dystrophy should be established as early as possible. In a survey of 83 families with 93 affected boys, the diagnosis was missed in every case referred to an orthopaedic surgeon (37 patients). In the whole group there was a mean delay of 2.0 years (0 to 6 years) during which time inappropriate treatment, difficulties in communication with parents, much parental anxiety and further pregnancies occurred. A serum creatine kinase estimation is a simple outpatient test which should be carried out on any boy with clumsy or abnormal gait, with flat feet or with an unexplained equinus deformity.

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Year:  1986        PMID: 3733820

Source DB:  PubMed          Journal:  J Bone Joint Surg Br        ISSN: 0301-620X


  4 in total

Review 1.  Evidence based case report: Assessing developmental delay.

Authors:  J Dorling; A Salt
Journal:  BMJ       Date:  2001-07-21

2.  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

3.  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

4.  Trendelenburg-Like Gait, Instability and Altered Step Patterns in a Mouse Model for Limb Girdle Muscular Dystrophy 2i.

Authors:  Joseph W Maricelli; Qi L Lu; David C Lin; Buel D Rodgers
Journal:  PLoS One       Date:  2016-09-14       Impact factor: 3.240

  4 in total

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