Refsumova nemoc [Refsum Disease]

tematický
6
Termíny

Refsumova choroba
Refsumova choroba - deficit fytanoyl CoA oxidasy
Refsumův syndrom

 

Adult Refsum Disease
Classic Refsum Disease
Hemeralopia Heredoataxia Polyneuritiformis
Hereditary Motor And Sensory Neuropathy IV
Hereditary Motor and Sensory Neuropathy Type IV
Hereditary Motor and Sensory Neuropathy, Type IV
Hereditary Type IV Motor and Sensory Neuropathy
Heredopathia Atactica Polyneuritiformis
HMSN 4
HMSN IV
HMSN Type IV
Neuropathy, Hereditary Motor and Sensory, Type IV
Phytanic Acid Oxidase Deficiency
Phytanic Acid Storage Disease
Refsum Disease, Adult
Refsum Disease, Classic
Refsum Disease, Phytanic Acid Oxidase Deficiency
Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency
Refsum Syndrome
Refsum-Thiebaut Syndrome
Refsum's Disease
Refsum's Syndrome

Perzistentní odkaz   https://www.medvik.cz/link/D012035
Definice

Refsumova nemoc - peroxizomální nemoc způsobená vrozenou defektní syntézou peroxizomů. Novorozenci vykazují dysmorfismus obličeje. Typická je ataxie, porucha kognitivních funkcí, postižení jater (mikronodulární cirhóza), hypercholesterolemie a sítnice. Častá je porucha sluchu. Chondrodysplazie a cystické změny v ledvinách chybí. Postižení jedinci se dožívají kolem 20 let života. (cit. Velký lékařský slovník online, 2013 http://lekarske.slovniky.cz/ )

An autosomal recessive familial disorder that usually presents in childhood with POLYNEUROPATHY; SENSORINEURAL HEARING LOSS; ICHTHYOSIS; ATAXIA; RETINITIS PIGMENTOSA; and CARDIOMYOPATHIES. (From Joynt, Clinical Neurology, 1991, Ch37, p58-9; Rev Med Interne 1996;17(5):391-8) This condition can be caused by mutation in the genes encoding peroxisomal phytanoyl-CoA hydroxylase or proteins associated peroxisomal membrane, leading to impaired catabolism of PHYTANIC ACID in PEROXISOMES.

Anotace
do not confuse with REFSUM DISEASE, INFANTILE
DUI
D012035 MeSH Prohlížeč
CUI
M0018709
Historická pozn.
1996 (1964)
Veřejná pozn.
1996; see REFSUM'S SYNDROME 1991-1995, see REFSUM DISEASE 1964-1990

C Nemoci
C10.228.140 nemoci mozku 1 178
C10.228.140.163 metabolické nemoci mozku 84
C10.228.140.163.100.084 adrenoleukodystrofie 41
C10.228.140.163.100.320 galaktosemie 44
C10.228.140.163.100.355 Hartnupova nemoc 2
C10.228.140.163.100.360 hepatolentikulární degenerace 243
C10.228.140.163.100.362 dědičné demyelinizační nemoci CNS 11
C10.228.140.163.100.365 homocystinurie 107
C10.228.140.163.100.375 neketotická hyperglycinemie 7
C10.228.140.163.100.380 hyperlysinemie
C10.228.140.163.100.412 Leighova nemoc 26
C10.228.140.163.100.425 Leschův-Nyhanův syndrom 20
C10.228.140.163.100.520 nemoc s močí javorového sirupu 8
C10.228.140.163.100.535 syndrom MELAS 17
C10.228.140.163.100.540 Menkesova choroba 12
C10.228.140.163.100.545 syndrom MERRF 4
C10.228.140.163.100.593 nedostatek mevalonátkinázy 16
C10.228.140.163.100.640 okulocerebrorenální syndrom 9
C10.228.140.163.100.687 fenylketonurie 285
C10.228.140.163.100.725 nedostatek pyruvátkarboxylázy
C10.228.140.163.100.813 Refsumova nemoc 6
C10.228.140.163.100.844 Refsumova nemoc infantilní
C10.228.140.163.100.875 tyrosinemie 18
C10.228.140.163.100.937 vrozené poruchy cyklu močoviny 7
C10.228.140.163.100.968 Zellwegerův syndrom 10
C10.500.300.099 Alströmův syndrom 1
C10.500.300.780 Refsumova nemoc 6
C10.574.500.495.099 Alströmův syndrom 1
C10.574.500.495.200 Charcotova-Marieova-Toothova nemoc 159
C10.574.500.495.780 Refsumova nemoc 6
C10.574.500.495.820 spastická paraplegie dědičná 23
C10.668.829.800 polyneuropatie 343
C10.668.829.800.300.099 Alströmův syndrom 1
C10.668.829.800.300.200 Charcotova-Marieova-Toothova nemoc 159
C10.668.829.800.300.780 Refsumova nemoc 6
C10.668.829.800.300.820 spastická paraplegie dědičná 23
C16.131 vrozené vady 1 741
C16.131.666.300.099 Alströmův syndrom 1
C16.131.666.300.200 Charcotova-Marieova-Toothova nemoc 159
C16.131.666.300.780 Refsumova nemoc 6
C16.131.666.300.820 spastická paraplegie dědičná 23
C16.320.400.375.099 Alströmův syndrom 1
C16.320.400.375.200 Charcotova-Marieova-Toothova nemoc 159
C16.320.400.375.780 Refsumova nemoc 6
C16.320.400.375.820 spastická paraplegie dědičná 23
C16.320.565.189.084 adrenoleukodystrofie 41
C16.320.565.189.320 galaktosemie 44
C16.320.565.189.355 Hartnupova nemoc 2
C16.320.565.189.360 hepatolentikulární degenerace 243
C16.320.565.189.365 homocystinurie 107
C16.320.565.189.375 neketotická hyperglycinemie 7
C16.320.565.189.380 hyperlysinemie
C16.320.565.189.412 Leighova nemoc 26
C16.320.565.189.425 Leschův-Nyhanův syndrom 20
C16.320.565.189.535 syndrom MELAS 17
C16.320.565.189.540 Menkesova choroba 12
C16.320.565.189.545 syndrom MERRF 4
C16.320.565.189.593 nedostatek mevalonátkinázy 16
C16.320.565.189.640 okulocerebrorenální syndrom 9
C16.320.565.189.687 fenylketonurie 285
C16.320.565.189.813 Refsumova nemoc 6
C16.320.565.189.844 Refsumova nemoc infantilní
C16.320.565.189.875 tyrosinemie 18
C16.320.565.189.968 Zellwegerův syndrom 10
C16.320.565.663 peroxizomální poruchy 20
C16.320.565.663.050 akatalázie 3
C16.320.565.663.100 adrenoleukodystrofie 41
C16.320.565.663.430 nedostatek mevalonátkinázy 16
C16.320.565.663.760 Refsumova nemoc 6
C16.320.565.663.865 Refsumova nemoc infantilní
C16.320.565.663.970 Zellwegerův syndrom 10
C18.452 metabolické nemoci 1 196
C18.452.132.100.084 adrenoleukodystrofie 41
C18.452.132.100.320 galaktosemie 44
C18.452.132.100.355 Hartnupova nemoc 2
C18.452.132.100.360 hepatolentikulární degenerace 243
C18.452.132.100.365 homocystinurie 107
C18.452.132.100.375 neketotická hyperglycinemie 7
C18.452.132.100.380 hyperlysinemie
C18.452.132.100.412 Leighova nemoc 26
C18.452.132.100.425 Leschův-Nyhanův syndrom 20
C18.452.132.100.535 syndrom MELAS 17
C18.452.132.100.540 Menkesova choroba 12
C18.452.132.100.545 syndrom MERRF 4
C18.452.132.100.593 nedostatek mevalonátkinázy 16
C18.452.132.100.640 okulocerebrorenální syndrom 9
C18.452.132.100.687 fenylketonurie 285
C18.452.132.100.813 Refsumova nemoc 6
C18.452.132.100.844 Refsumova nemoc infantilní
C18.452.132.100.875 tyrosinemie 18
C18.452.132.100.968 Zellwegerův syndrom 10
C18.452.648.189.084 adrenoleukodystrofie 41
C18.452.648.189.320 galaktosemie 44
C18.452.648.189.355 Hartnupova nemoc 2
C18.452.648.189.360 hepatolentikulární degenerace 243
C18.452.648.189.365 homocystinurie 107
C18.452.648.189.375 neketotická hyperglycinemie 7
C18.452.648.189.380 hyperlysinemie
C18.452.648.189.412 Leighova nemoc 26
C18.452.648.189.425 Leschův-Nyhanův syndrom 20
C18.452.648.189.535 syndrom MELAS 17
C18.452.648.189.540 Menkesova choroba 12
C18.452.648.189.545 syndrom MERRF 4
C18.452.648.189.593 nedostatek mevalonátkinázy 16
C18.452.648.189.640 okulocerebrorenální syndrom 9
C18.452.648.189.687 fenylketonurie 285
C18.452.648.189.813 Refsumova nemoc 6
C18.452.648.189.844 Refsumova nemoc infantilní
C18.452.648.189.875 tyrosinemie 18
C18.452.648.189.968 Zellwegerův syndrom 10
C18.452.648.663 peroxizomální poruchy 20
C18.452.648.663.050 akatalázie 3
C18.452.648.663.100 adrenoleukodystrofie 41
C18.452.648.663.430 nedostatek mevalonátkinázy 16
C18.452.648.663.760 Refsumova nemoc 6
C18.452.648.663.865 Refsumova nemoc infantilní
C18.452.648.663.970 Zellwegerův syndrom 10

Neuropathy, hereditary motor and sensory, LOM type Disease MeSH Prohlížeč

Refsum Disease, Adult, 1 Disease MeSH Prohlížeč

Refsum Disease, Adult, 2 Disease MeSH Prohlížeč

Refsum disease with increased pipecolic acidemia Disease MeSH Prohlížeč