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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.500 Myotonic Dystrophy .
C05.651.662 Myotonic Disorders .
C05.651.662.500 Myotonia Congenita .
C05.651.662.750 Myotonic Dystrophy .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.545 Myotonia Congenita .
C10.574.500.547 Myotonic Dystrophy .
C10.597 Neurologic Manifestations .
C10.597.613 Neuromuscular Manifestations .
C10.597.613.700 Myotonia .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.500 Myotonic Dystrophy .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.500 Myotonia Congenita .
C10.668.491.606.750 Myotonic Dystrophy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.540 Myotonia Congenita .
C16.320.400.542 Myotonic Dystrophy .
C16.320.577 Muscular Dystrophies .
C16.320.577.500 Myotonic Dystrophy .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.608 Neuromuscular Manifestations .
C23.888.592.608.700 Myotonia .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Myotonia Congenita .
Batten Turner Congenital Myopathy .
Batten-Turner Congenital Myopathy .
Becker Disease .
Congenital Myotonia .
Generalized Myotonia of Becker .
Generalized Myotonia of Thomsen .
Myopathy, Congenital .
Myotonia Congenita, Autosomal Dominant .
Myotonia Congenita, Autosomal Recessive .
Myotonia Levior .
Myotonia, Generalized .
Thomsen's Disease .
Thomsens Disease .
Disease, Becker .
Disease, Thomsen .
Disease, Thomsen's .
Disease, Thomsens .
Generalized Myotonia .
Generalized Myotonia, Becker .
Generalized Myotonias .
Myotonia, Becker Generalized .
Myotonias, Generalized .
Thomsen Generalized Myotonia .
Thomsen Disease .
Becker Generalized Myotonia .
Myotonia, Generalized, Becker .
THOMSEN'S DISEASE .
Inherited myotonic disorders with early childhood onset MYOTONIA. Muscular hypertrophy is common and myotonia may impair ambulation and other movements. It is classified as Thomsen (autosomal dominant) or Becker (autosomal recessive) generalized myotonia mainly based on the inheritance pattern. Becker type is also clinically more severe. An autosomal dominant variant with milder symptoms and later onset is known as myotonia levior. Mutations in the voltage-dependent skeletal muscle chloride channel are associated with the disorders. .
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Myotonic Dystrophy .
Congenital Myotonic Dystrophy .
Dystrophia Myotonica 1 .
Dystrophia Myotonica 2 .
Myotonia Atrophica .
Myotonia Dystrophica .
Myotonic Dystrophy 1 .
Myotonic Dystrophy 2 .
PROMM (Proximal Myotonic Myopathy) .
Proximal Myotonic Myopathy .
Ricker Syndrome .
Steinert Myotonic Dystrophy .
Steinert's Disease .
Atrophica, Myotonia .
Atrophicas, Myotonia .
Congenital Myotonic Dystrophies .
Disease, Steinert .
Disease, Steinert's .
Dystrophia Myotonica 2s .
Dystrophia Myotonicas .
Dystrophica, Myotonia .
Dystrophicas, Myotonia .
Dystrophies, Congenital Myotonic .
Dystrophies, Myotonic .
Dystrophy, Congenital Myotonic .
Dystrophy, Myotonic .
Dystrophy, Steinert Myotonic .
Myopathies, Proximal Myotonic .
Myopathy, Proximal Myotonic .
Myotonia Atrophicas .
Myotonia Dystrophicas .
Myotonic Dystrophies .
Myotonic Dystrophies, Congenital .
Myotonic Dystrophy, Steinert .
Myotonic Myopathies, Proximal .
Myotonica, Dystrophia .
Myotonicas, Dystrophia .
PROMMs (Proximal Myotonic Myopathy) .
Proximal Myotonic Myopathies .
Steinerts Disease .
Syndrome, Ricker .
Dystrophia Myotonica .
Steinert Disease .
Myotonic Dystrophy, Congenital .
Myotonic Myopathy, Proximal .
MYOTONIA DYSTROPHICA .
STEINERT'S DISEASE .
MYOTONIA ATROPHICA .
Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. .
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Neuromuscular Diseases .
Cramp-Fasciculation Syndrome .
Fasciculation-Cramp Syndrome, Benign .
Foley-Denny-Brown Syndrome .
Oppenheim's Disease .
Benign Fasciculation-Cramp Syndrome .
Benign Fasciculation-Cramp Syndromes .
Cramp Fasciculation Syndrome .
Cramp-Fasciculation Syndromes .
Fasciculation Cramp Syndrome, Benign .
Fasciculation-Cramp Syndromes, Benign .
Foley Denny Brown Syndrome .
Neuromuscular Disease .
Oppenheims Disease .
Syndrome, Cramp-Fasciculation .
Syndrome, Foley-Denny-Brown .
Syndromes, Cramp-Fasciculation .
Amyotonia Congenita .
Oppenheim Disease .
MYATONIA CONGENITA .
OPPENHEIM'S DISEASE .
A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. .
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Myotonia .
Myotonic Phenomenon .
Percussion Myotonia .
Myotonia, Percussion .
Myotonias .
Myotonias, Percussion .
Myotonic Phenomenons .
Percussion Myotonias .
Phenomenon, Myotonic .
Phenomenons, Myotonic .
Prolonged failure of muscle relaxation after contraction. This may occur after voluntary contractions, muscle percussion, or electrical stimulation of the muscle. Myotonia is a characteristic feature of MYOTONIC DISORDERS. .
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