Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East.

Alghamdi, Fouad; Al-Tawari, Asmaa; Alrohaif, Hadil; Alshuaibi, Walaa; Mansour, Hicham; Aartsma-Rus, Annemieke; Mégarbané, André

Alghamdi, Fouad; Al-Tawari, Asmaa; Alrohaif, Hadil; Alshuaibi, Walaa; Mansour, Hicham; Aartsma-Rus, Annemieke; Mégarbané, André.

Afiliación

Alghamdi F; Neuroscience Center, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Al-Tawari A; Pediatric Neurology Unit, Pediatric Department, Al-Sabah Hospital, Kuwait City, Kuwait.
Alrohaif H; Kuwait Medical Genetics Centre, Al-Sabah Hospital, Kuwait City, Kuwait.
Alshuaibi W; College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mansour H; Medical Genetics Division, Pediatrics Department, King Saud University, Riyadh, Saudi Arabia.
Aartsma-Rus A; Pediatric Department, Saint George Hospital, Balamand University, Beirut, Lebanon.
Mégarbané A; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.

Front Pediatr ; 9: 716424, 2021.

Article en En | MEDLINE | ID: mdl-34595143

Palabras clave

DMD; case report; diagnostic delay; genetic diagnosis; neuromuscular disorder

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline Aspecto: Patient_preference Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Suiza

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