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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.662 Myotonic Disorders .
C05.651.662.500 Myotonia Congenita .
C05.651.701 Paralyses, Familial Periodic .
C05.651.701.600 Paralysis, Hyperkalemic Periodic .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.545 Myotonia Congenita .
C10.597 Neurologic Manifestations .
C10.597.622 Paralysis .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.500 Myotonia Congenita .
C10.668.491.650 Paralyses, Familial Periodic .
C10.668.491.650.600 Paralysis, Hyperkalemic Periodic .
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 .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.711 Paralyses, Familial Periodic .
C16.320.565.618.711.600 Paralysis, Hyperkalemic Periodic .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.711 Paralyses, Familial Periodic .
C18.452.648.618.711.600 Paralysis, Hyperkalemic Periodic .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.636 Paralysis .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Myotonic Disorders .
Eulenburg Disease .
Eulenburg's Disease .
Paralysis Periodica Paramyotonia .
Paramyotonia Congenita Without Cold Paralysis .
Paramyotonia Congenita of von Eulenberg .
Von Eulenberg's Disease .
Disorder, Myotonic .
Disorders, Myotonic .
Myopathy, Myotonic .
Myotonic Disorder .
Myotonic Myopathies .
Myotonic Myopathy .
Von Eulenberg Disease .
Myopathies, Myotonic .
Myotonia Fluctuans .
Paramyotonia Congenita .
Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. .
1.00
2242
 
Paralysis .
Todd Paralysis .
Todd's Paralysis .
Palsies .
Paralyses .
Paralysis, Todd .
Paralysis, Todd's .
Plegias .
Todds Paralysis .
Palsy .
Plegia .
PSEUDOBULBAR PARALYSIS .
A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) .
0.54
22614892
 
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. .
0.50
2489320
 
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. .
0.48
14753
 
Paralysis, Hyperkalemic Periodic .
Adynamia Episodica Hereditaria .
Adynamia Episodica Hereditaria with or without Myotonia .
Familial Hyperkalemic Periodic Paralysis .
Gamstorp Disease .
Gamstorp Episodic Adynamy .
HyperKPP .
HyperPP .
Hyperkalemic Periodic Paralysis Type 2 .
Hyperkalemic Periodic Paralysis, Familial .
Hyperkaliemic Periodic Paralysis Type 2 .
Primary Hyperkalemic Periodic Paralysis .
Sodium Channel Muscle Disease .
Disease, Gamstorp .
Hyperkalemic Periodic Paralysis .
Myotonic Periodic Paralysis .
Paralysis, Periodic, Hyperkalemic, Familial .
An autosomal dominant familial disorder which presents in infancy or childhood and is characterized by episodes of weakness associated with hyperkalemia. During attacks, muscles of the lower extremities are initially affected, followed by the lower trunk and arms. Episodes last from 15-60 minutes and typically occur after a period of rest following exercise. A defect in skeletal muscle sodium channels has been identified as the cause of this condition. Normokalemic periodic paralysis is a closely related disorder marked by a lack of alterations in potassium levels during attacks of weakness. (Adams et al., Principles of Neurology, 6th ed, p1481) .
0.45
192