DergiPark: 378994tmsjIntroduction: Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscular dystrophy which starts with shoulder and face muscles involvement and rarely spreads to pelvic muscles. It has autosomal dominant inheritance pattern, serum CK levels are normal or mildly high, and EMG is myopathic. Case report:We present the 43 year old male patient with pain, numbness and weakness in cervical area and both arms for 1 year. His mother has similar symptoms as well. His cervical spinal nerve EMG results were found normal. Results:EMG results were found normal. Our patient had the defect of closing eyelids or pressing them based on faced muscles involvement just like regular FSHD cases. Because of the atrophy of lo...
Facioscapulohumeral muscular dystrophy (FSHD) is an inherited and progressive muscle disorder. Altho...
AbstractIntroductionFacioScapuloHumeral Muscular Dystrophy (FSHD), a disease linked to a heterozygou...
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular de...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant, inherited disorder character...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Two patients developed progressive muscle weakness in adult life. The initial diagnosis of polymyosi...
Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease...
Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease...
Contains fulltext : 87385.pdf (publisher's version ) (Closed access)Facioscapulohu...
A 77-year-old male is presented. He had onset of proximal weakness 10 years earlier. His course was ...
Background: We report on a patient with genetically confirmed overlapping diagnoses of CMT1A and FSH...
We report a patient with early onset facioscapulohumeral muscular dystrophy type 1 (FSHD1) who was n...
Contains fulltext : 232742.pdf (Publisher’s version ) (Open Access)OBJECTIVE: To e...
Artículo de publicación ISIBackground: Facioscapulohumeral muscular dystrophy is the third most com...
Facioscapulohumeral muscular dystrophy (FSHD) is an inherited and progressive muscle disorder. Altho...
AbstractIntroductionFacioScapuloHumeral Muscular Dystrophy (FSHD), a disease linked to a heterozygou...
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular de...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant, inherited disorder character...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Two patients developed progressive muscle weakness in adult life. The initial diagnosis of polymyosi...
Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease...
Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease...
Contains fulltext : 87385.pdf (publisher's version ) (Closed access)Facioscapulohu...
A 77-year-old male is presented. He had onset of proximal weakness 10 years earlier. His course was ...
Background: We report on a patient with genetically confirmed overlapping diagnoses of CMT1A and FSH...
We report a patient with early onset facioscapulohumeral muscular dystrophy type 1 (FSHD1) who was n...
Contains fulltext : 232742.pdf (Publisher’s version ) (Open Access)OBJECTIVE: To e...
Artículo de publicación ISIBackground: Facioscapulohumeral muscular dystrophy is the third most com...
Facioscapulohumeral muscular dystrophy (FSHD) is an inherited and progressive muscle disorder. Altho...
AbstractIntroductionFacioScapuloHumeral Muscular Dystrophy (FSHD), a disease linked to a heterozygou...
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular de...