Prenatal Diagnosis of the Duchenne Muscular Dystrophy. A Family Presentation
The Duchenne muscular dystrophy is one of the most frequent hereditary myopathies that exist. It is characterized by degeneration of the muscle skeletal fibers which produce handicap in the first decade of life bringing about death due to cardiac or respiratory failure. The responsible gene of the d...
Saved in:
Main Authors: | Humberto Perera Navarro, Tatiana Zaldivar-Vaillant, Carlos Viñas-Portilla, Ariel Medina Concepción, Rosa Guerra Badía, Mariesky Zayas Guillot |
---|---|
Format: | Article |
Language: | Spanish |
Published: |
Centro Provincial de Información de Ciencias Médicas. Cienfuegos
2007-05-01
|
Series: | Medisur |
Subjects: | |
Online Access: | http://medisur.sld.cu/index.php/medisur/article/view/247 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Diagnóstico molecular de distrofia muscular de Duchenne/Becker en una familia sin antecedentes patológicos de la enfermedad
by: Ivonne Martín Hernández, et al.
Published: (2018-10-01) -
Bone measurements interact with phenotypic measures in canine Duchenne muscular dystrophy
by: Sarah M. Schneider, et al.
Published: (2025-01-01) -
Unraveling the Genetic Heartbeat: Decoding Cardiac Involvement in Duchenne Muscular Dystrophy
by: Valeria Novelli, et al.
Published: (2025-01-01) -
Distrofia muscular de cinturas tipo 2C (LGMD2C)
by: Sandra Milena Zuleta Alarcón, et al.
Published: (2025-01-01) -
Pharmacological interventions for the management of anesthesia and sedation in patients with Duchenne muscular dystrophy: a systematic review and meta-analysis
by: Xianghong Lian, et al.
Published: (2025-01-01)