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Updated: Sep 10, 2025

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Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
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Tres casos de embarazos complicados con distrofia miotónica tipo 1
Asako Kumagai1, Yusen Sugimura1, Satomi Tanaka1
1Department of Obstetrics and Gynecology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
The journal of obstetrics and gynaecology research
|August 23, 2025
Resumen
La distrofia miotónica congénita tipo 1 (DM1) puede causar complicaciones neonatales graves. El aumento de la creatinina fosfoquinasa sérica (CPK) puede indicar la DM1 materna, incluso sin los signos de advertencia típicos del embarazo.
Área de la Ciencia:
- Neurología
- La genética
- Obstetricia y parto
Sus antecedentes:
- La distrofia miotónica tipo 1 (DM1) es un trastorno neuromuscular genético.
- La expansión repetida del trinucleótido causa DM1.
- Los embarazos en mujeres con DM1 se enfrentan a mayores riesgos, especialmente para la DM1 congénita con síntomas neonatales graves.
Palabras clave:
Trastornos congénitosLa creatina fosfoquinasaDistrofia miotónica 1Polyhydramnios, también conocido como polihidramniosembarazoMás Videos Relacionados
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