serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.050 Animals .
B01.050.500 Invertebrates .
B01.050.500.500 Helminths .
B01.050.500.500.736 Platyhelminths .
B01.050.500.500.736.215 Cestoda .
B01.050.500.500.736.215.895 Taenia .
B01.050.500.500.736.215.895.286 Cysticercus .
C03 Parasitic Diseases .
C03.105 Central Nervous System Parasitic Infections .
C03.105.250 Central Nervous System Helminthiasis .
C03.105.250.550 Neurocysticercosis .
C03.335 Helminthiasis .
C03.335.190 Cestode Infections .
C03.335.190.902 Taeniasis .
C03.335.190.902.185 Cysticercosis .
C03.335.190.902.185.550 Neurocysticercosis .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.228 Central Nervous System Infections .
C10.228.228.205 Central Nervous System Parasitic Infections .
C10.228.228.205.250 Central Nervous System Helminthiasis .
C10.228.228.205.250.550 Neurocysticercosis .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.377 Cystinosis .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.377 Cystinosis .
D01 Inorganic Chemicals .
D01.248 Electrolytes .
D01.248.497 Ions 5743 .
D01.248.497.158 Anions .
D01.248.497.158.874 Sulfides .
D01.248.497.158.874.390 Disulfides .
D01.248.497.158.874.390.369 Cystine .
D01.875 Sulfur Compounds .
D01.875.350 Hydrogen Sulfide .
D01.875.350.850 Sulfides .
D01.875.350.850.150 Disulfides .
D01.875.350.850.150.369 Cystine .
D02 Organic Chemicals .
D02.886 Sulfur Compounds .
D02.886.030 Amino Acids, Sulfur .
D02.886.030.230 Cysteine .
D02.886.030.230.369 Cystine .
D02.886.520 Sulfides .
D02.886.520.150 Disulfides .
D02.886.520.150.087 Cystine .
D12 Amino Acids, Peptides, and Proteins .
D12.125 Amino Acids .
D12.125.095 Amino Acids, Diamino .
D12.125.095.369 Cystine .
D12.125.119 Amino Acids, Dicarboxylic .
D12.125.119.369 Cystine .
D12.125.166 Amino Acids, Sulfur .
D12.125.166.230 Cysteine .
D12.125.166.230.369 Cystine .
SP4 Environmental Health .
SP4.001 Health .
SP4.001.012 Environmental Illness .
SP4.001.012.138 Parasitic Diseases .
SP4.001.012.138.119 Helminthiasis .
SP4.001.012.138.119.065 Cysticercosis .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Cysticercosis .
Cysticercoses .
Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. .
1.00
 
Neurocysticercosis .
Brain Cysticercosis .
Neurocysticercoses .
Cysticercosis, Brain .
Central Nervous System Cysticercosis .
Cysticercosis, Central Nervous System .
Infection of the brain, spinal cord, or perimeningeal structures with the larval forms of the genus TAENIA (primarily T. solium in humans). Lesions formed by the organism are referred to as cysticerci. The infection may be subacute or chronic, and the severity of symptoms depends on the severity of the host immune response and the location and number of lesions. SEIZURES represent the most common clinical manifestation although focal neurologic deficits may occur. (From Joynt, Clinical Neurology, 1998, Ch27, pp46-50) .
0.82
 
Cysticercus .
The larval form of various tapeworms of the genus Taenia. .
0.76
96895
 
Cystinosis .
Cystine Diathesis .
Cystine Disease .
Cystine Storage Disease .
Cystinoses .
Cystinosin, Defect of .
Cystinosis, Nephropathic .
Lysosomal Cystine Transport Protein, Defect Of .
Nephropathic Cystinosis .
Cystine Diatheses .
Cystine Diseases .
Cystine Storage Diseases .
Cystinoses, Nephropathic .
Defect of Cystinosin .
Defect of Cystinosins .
Diatheses, Cystine .
Diathesis, Cystine .
Nephropathic Cystinoses .
Storage Disease, Cystine .
Storage Diseases, Cystine .
A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME. .
0.66
 
Cystine .
Copper Cystinate .
L-Cystine .
L Cystine .
A covalently linked dimeric nonessential amino acid formed by the oxidation of CYSTEINE. Two molecules of cysteine are joined together by a disulfide bridge to form cystine. .
0.62
265010