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Spinal muscular atrophy - Wikipedia, the free encyclopedia
Spinal Muscular Atrophy ( SMA ) is a neuromuscular disease characterized by degeneration of motor neurons, resulting in progressive muscular atrophy (wasting away) and weakness. The clinical spectr...
en.wikipedia.org/wiki/Spinal_muscular_atrophy |
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Spinal muscular atrophy (SMA), the number one genetic killer of children under the age of two, is an often fatal disease that destroys the nerves controlling voluntary muscle movement, which affects crawling, walking, head and neck control, and even swallowing. ... Type I, or Werdnig-Hoffmann Disease, is the most severe...
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Overview of Spinal muscular atrophy type 2 as a medical condition including introduction, prevalence, prognosis, profile, symptoms, diagnosis, misdiagnosis, and treatment ... Symptoms of Spinal muscular atrophy type 2...
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Overview of Spinal muscular atrophy type 2 as a medical condition including introduction, prevalence, prognosis, profile, symptoms, diagnosis, misdiagnosis, and treatment ... Symptoms of Spinal muscular atrophy type 2...
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Spinal muscular atrophy (SMA) is the second leading cause of neuromuscular disease. It is inherited as an ... In its most severe form (SMA type I, also called Werdnig-Hoffman disease), infants are born floppy with weak, thin muscles and feeding and breathing problems. Their lifespan seldom exceeds 2 to 3 years.
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Distal spinal muscular atrophy (spinal CMT or HMN type II): This may clinically mimic Charcot-Marie-Tooth (CMT) disease, otherwise known as hereditary motor and sensory neuropathy (HMSN) types 1 and 2: CMT is characterized by peroneal muscular atrophy, weakness, and wasting in the legs.
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OBJECTIVE: To determine the major complication rate in the first 30 days after enterostomy tube insertion in infants with spinal muscular atrophy (SMA) type 1. STUDY DESIGN: A retrospective case review of all children with SMA type 1 who had a gastrostomy or gastrojejunostomy tube placed by the image-guided technique...
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