THE “MUSCULAR SYNDROME”
نویسندگان
چکیده
منابع مشابه
Muscular involvement in the Holt-Oram syndrome.
Holt-Oram syndrome is an autosomal dominant disorder characterised by radial ray and congenital heart defects. Recently, a gene for this disorder has been identified on chromosome 12q24.1, encoding a T box transcription factor. However, the functional role of the gene product is not completely understood. We present results of neurological, radiological, and muscle magnetic resonance imaging (M...
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1Department of Neurology, Medical School of the University of São Paulo, São Paulo SP, Brazil; 2Department of Ophthalmology, Medical School of the University of São Paulo, São Paulo SP, Brazil. Correspondence: Lívia MA Pasqualin; Department of Neurology, Medical School of the USP; Avenida Dr. Enéas de Carvalho Aguiar 255 / sala 5131; 05403-000 São Paulo SP Brasil; E-mail: [email protected]...
متن کاملChildhood Muscular Fitness Phenotypes and Adult Metabolic Syndrome.
PURPOSE The objective of this study is to determine whether childhood muscular fitness phenotypes (strength, endurance, and power) are independently associated with adult metabolic syndrome (MetS). METHODS We conducted a longitudinal study including 737 participants who had muscular fitness measures in 1985 when age 9, 12, or 15 yr and attended follow-up in young adulthood 20 yr later when me...
متن کاملSegmental muscular atrophy in a patient with post polio syndrome.
A 53-year-old man complained of atrophy of his left leg persisting for three years. Although he had suffered from poliomyelitis at the age of two, he had experienced no weakness for almost fifty years since complete recovery of poliomyelitis. There was no bulbar palsy or sensory deficit. Deep tendon reflexes were decreased in the lower limbs. Nerve conduction study was normal. Electromyography ...
متن کاملIntermittent Pre-Excitation-Syndrome in Facio-Scapulo-Humeral Muscular Dystrophy
Pre-excitation-syndrome has not been reported as a phenotypic feature of facio-scapulo-humeral muscular dystrophy (FSH-MD). In a 39-year-old male with FSH-MD due to a reduced tandem repeat size in the D4Z4-locus on chromosome 4q35, cardiac involvement, manifesting as an incomplete right bundle-branch-block, tall T-waves in V 3-5, ST-elevation in V 2-4, and mild thickening of the left ventricula...
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ژورنال
عنوان ژورنال: The Journal OF Nervous and Mental Disease
سال: 1920
ISSN: 0022-3018
DOI: 10.1097/00005053-192007000-00038