Multi‐parametric MR in Becker muscular dystrophy patients
نویسندگان
چکیده
منابع مشابه
Valley sign in Becker muscular dystrophy and outliers of Duchenne and Becker muscular dystrophy.
Valley sign has been described in patients with Duchenne muscular dystrophy (DMD). As there are genetic and clinical similarities between DMD and Becker muscular dystrophy (BMD), this clinical sign is evaluated in this study in BMD and DMD/BMD outliers. To evaluate the sign, 28 patients with Becker muscular dystrophy (BMD), 8 DMD/BMD outliers and 44 age-matched male controls with other neuromus...
متن کاملCardiac resynchronization therapy in becker muscular dystrophy: for which patients?
University of Medicine and Dentistry of New Jersey, 401, Haddon Avenue Camden, New Jersey, USA e-mail: fayssoil2000@ yahoo.fr
متن کاملCardiac resynchronization therapy in becker muscular dystrophy.
A 44-year-old male patient with known Becker muscular dystrophy and concomitant non-ischemic dilated cardiomyopathy presented to our department because of worsening heart failure and presyncope. Upon admission, the patient was in New York Heart Association functional class III despite optimal pharmacological treatment; his ECG showed sinus rhythm with left bundle branch block and a wide QRS com...
متن کاملmolecular diagnosis of duchene/ becker muscular dystrophy in iranian patients
duchene and becker muscular dystrophy (dmd and bmd) are x-linked conditions that result from a defect in the dystrophin gene located on xp21. dmd is the most frequent neuromuscular disease in humans (1/3500 male newborns). in approximately 65% of dmd and bmd patients, deletions in the dystrophin gene have been identified as the molecular determinant. population-based variations in frequency and...
متن کاملDystrophin-related protein in Becker muscular dystrophy.
A benign Becker muscular dystrophy (BMD) patient with a marked decrease in dystrophin exhibited remarkable expression of dystrophin-related protein (DRP) on most of the muscle cell membrane. A phenotypic Duchenne muscular dystrophy patient with a truncated form of dystrophin exhibited no DRP expression on the muscle cell membrane except for the neuromuscular junction. Increased DRP expression m...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: NMR in Biomedicine
سال: 2020
ISSN: 0952-3480,1099-1492
DOI: 10.1002/nbm.4385