Time to Diagnosis of Duchenne Muscular Dystrophy Patients With or Without Development Delay

IntroductionDuchenne muscular dystrophy, the most common inherited neuromuscular disease in children, typically presents its first symptoms at 3-5 years of age with progressive muscular weakness. However, in some boys, the disease manifests earlier in childhood with developmental delays, such as delays in walking and speech, or signs of an autism spectrum disorder.ObjectiveTo analyze and compare the age and time until diagnosis in boys with Duchenne muscular dystrophy, with or without developmental delays as the first sign of disease.Material and MethodsThis is a retrospective descriptive study. Data were collected from 127 boys with Duchenne muscular dystrophy who were followed at the Outpatient Muscle Clinic of Hospital das Clínicas (FMUSP/SP) from 2015 to 2024. To determine the age and time interval between symptom onset and diagnosis, we analyzed the total sample, and 3 separate groups based on initial symptoms.ResultsIn the total sample, the mean age of diagnosis was 6.9 years, with an average interval of 3.6 years between symptom onset and diagnosis. In patients with developmental delays, initial symptoms were observed at an average age of 1.4 years, and despite a diagnosis delay of 3.4 years, these patients were diagnosed an average of 2.7 years earlier than those with normal development.ConclusionOur findings suggest that Duchenne muscular dystrophy should be considered in the differential diagnosis of boys presenting with developmental delays (motor, speech, or cognitive). In such cases, screening with creatine kinase level measurements is crucial.

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Publication Details

Journal
Journal of Child Neurology
Published
2025-06-18
DOI
https://doi.org/10.1177/08830738251346285
Citations
1
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.81
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article

Time to Diagnosis of Duchenne Muscular Dystrophy Patients With or Without Development Delay

Karlla Danielle Ferreira Lima, Marco Antônio Veloso de Albuquerque, Edmar Zanoteli, Fernando Kok
1 citations
Journal of Child Neurology
Muscle Physiology and Disorders
0.81
article

Time to Diagnosis of Duchenne Muscular Dystrophy Patients With or Without Development Delay

Karlla Danielle Ferreira Lima, Marco Antônio Veloso de Albuquerque, Edmar Zanoteli, Fernando Kok
article en
1 citations

Abstract

IntroductionDuchenne muscular dystrophy, the most common inherited neuromuscular disease in children, typically presents its first symptoms at 3-5 years of age with progressive muscular weakness. However, in some boys, the disease manifests earlier in childhood with developmental delays, such as delays in walking and speech, or signs of an autism spectrum disorder.ObjectiveTo analyze and compare the age and time until diagnosis in boys with Duchenne muscular dystrophy, with or without developmental delays as the first sign of disease.Material and MethodsThis is a retrospective descriptive study. Data were collected from 127 boys with Duchenne muscular dystrophy who were followed at the Outpatient Muscle Clinic of Hospital das Clínicas (FMUSP/SP) from 2015 to 2024. To determine the age and time interval between symptom onset and diagnosis, we analyzed the total sample, and 3 separate groups based on initial symptoms.ResultsIn the total sample, the mean age of diagnosis was 6.9 years, with an average interval of 3.6 years between symptom onset and diagnosis. In patients with developmental delays, initial symptoms were observed at an average age of 1.4 years, and despite a diagnosis delay of 3.4 years, these patients were diagnosed an average of 2.7 years earlier than those with normal development.ConclusionOur findings suggest that Duchenne muscular dystrophy should be considered in the differential diagnosis of boys presenting with developmental delays (motor, speech, or cognitive). In such cases, screening with creatine kinase level measurements is crucial.

Journal of Child NeurologyVol. 41(1)
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR)
Good health and well-being
Openalex Percentile: Top 27%
Muscle Physiology and Disorders
0.81
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Time to Diagnosis of Duchenne Muscular Dystrophy Patients With or Without Development Delay — Karlla Danielle Ferreira Lima, Marco Antônio Veloso de Albuquerque, et al. · Journal of Child Neurology (2025) | TGRS Research Map | TGRS