Paralyses, Familial Periodic [paralýzy familiární periodické]

topical
7
Terms

normokalemická periodická paralýza

 

Familial Periodic Paralysis
Normokalemic Periodic Paralysis
Periodic Paralysis, Familial

Persistent link   https://www.medvik.cz/link/D010245
Definition

A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481)

Annotation
a specific disease entity: see MeSH definition
DUI
D010245 MeSH Browser
CUI
M0015880
History note
2000(1966)
Public note
2000; see PARALYSIS, FAMILIAL PERIODIC 1966-1999

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 2
CO
complications
CN
congenital
DI
diagnosis 5
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 2
GE
genetics 1
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C05 Musculoskeletal Diseases 1 120
C05.651 Muscular Diseases 553
C05.651.102 Arthrogryposis 31
C05.651.180 Compartment Syndromes 113
C05.651.197 Contracture 154
C05.651.243 Craniomandibular Disorders 9
C05.651.290 Eosinophilia-Myalgia Syndrome 3
C05.651.310 Fatigue Syndrome, Chronic 276
C05.651.324 Fibromyalgia 133
C05.651.392 Isaacs Syndrome 7
C05.651.426 Medial Tibial Stress Syndrome 2
C05.651.460 Mitochondrial Myopathies 40
C05.651.475 Muscle Cramp 176
C05.651.494 Muscle Neoplasms 17
C05.651.504 Muscle Rigidity 47
C05.651.512 Muscle Spasticity 457
C05.651.515 Muscle Weakness 224
C05.651.534 Muscular Disorders, Atrophic 45
C05.651.538 Musculoskeletal Pain 146
C05.651.542 Myalgia 53
C05.651.550 Myofascial Pain Syndromes 92
C05.651.575 Myopathies, Structural, Congenital 15
C05.651.594 Myositis 250
C05.651.662 Myotonic Disorders 23
C05.651.682 Myotoxicity 1
C05.651.701 Paralyses, Familial Periodic 7
C05.651.701.450 Hypokalemic Periodic Paralysis 6
C05.651.701.600 Paralysis, Hyperkalemic Periodic 2
C05.651.742 Polymyalgia Rheumatica 110
C05.651.807 Rhabdomyolysis 128
C05.651.869 Tendinopathy 90
C10 Nervous System Diseases 1 878
C10.668 Neuromuscular Diseases 330
C10.668.491 Muscular Diseases 553
C10.668.491.050 Eosinophilia-Myalgia Syndrome 3
C10.668.491.087 Medial Tibial Stress Syndrome 2
C10.668.491.175 Muscular Disorders, Atrophic 45
C10.668.491.425 Fibromyalgia 133
C10.668.491.500 Mitochondrial Myopathies 40
C10.668.491.525 Myalgia 53
C10.668.491.550 Myopathies, Structural, Congenital 15
C10.668.491.562 Myositis 250
C10.668.491.606 Myotonic Disorders 23
C10.668.491.628 Myotoxicity 1
C10.668.491.650 Paralyses, Familial Periodic 7
C10.668.491.650.450 Hypokalemic Periodic Paralysis 6
C10.668.491.650.600 Paralysis, Hyperkalemic Periodic 2
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.565 Metabolism, Inborn Errors 711
C16.320.565.618 Metal Metabolism, Inborn Errors 16
C16.320.565.618.337 Hemochromatosis 198
C16.320.565.618.403 Hepatolenticular Degeneration 243
C16.320.565.618.482 Hypophosphatasia 16
C16.320.565.618.544 Hypophosphatemia, Familial 12
C16.320.565.618.590 Menkes Kinky Hair Syndrome 12
C16.320.565.618.711 Paralyses, Familial Periodic 7
C16.320.565.618.711.550 Hypokalemic Periodic Paralysis 6
C16.320.565.618.711.600 Paralysis, Hyperkalemic Periodic 2
C16.320.565.618.815 Pseudohypoparathyroidism 31
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.648 Metabolism, Inborn Errors 711
C18.452.648.618 Metal Metabolism, Inborn Errors 16
C18.452.648.618.337 Hemochromatosis 198
C18.452.648.618.403 Hepatolenticular Degeneration 243
C18.452.648.618.482 Hypophosphatasia 16
C18.452.648.618.544 Hypophosphatemia, Familial 12
C18.452.648.618.590 Menkes Kinky Hair Syndrome 12
C18.452.648.618.711 Paralyses, Familial Periodic 7
C18.452.648.618.711.550 Hypokalemic Periodic Paralysis 6
C18.452.648.618.711.600 Paralysis, Hyperkalemic Periodic 2
C18.452.648.618.815 Pseudohypoparathyroidism 31

Normokalemic Periodic Paralysis, Potassium-Sensitive Disease MeSH Browser

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