Cockayneův syndrom [Cockayne Syndrome]

tematický
4
Termíny

Cockaynův syndrom I
Cockaynův syndrom II
Cockaynův syndrom III
klasický Cockaynův syndrom
Neill-Dingwallův syndrom

 

Cockayne Syndrome Type 3
Cockayne Syndrome Type C
Cockayne Syndrome, Group A
Cockayne Syndrome, Group B
Cockayne Syndrome, Group C
Cockayne Syndrome, Type A
Cockayne Syndrome, Type B
Cockayne Syndrome, Type C
Cockayne Syndrome, Type I
Cockayne Syndrome, Type II
Cockayne Syndrome, Type III
Dwarfism-Retinal Atrophy-Deafness Syndrome
Group A Cockayne Syndrome
Group B Cockayne Syndrome
Group C Cockayne Syndrome
Progeria-Like Syndrome
Progeroid Nanism
Type A Cockayne Syndrome
Type B Cockayne Syndrome
Type C Cockayne Syndrome
Type I Cockayne Syndrome
Type II Cockayne Syndrome
Type III Cockayne Syndrome

Perzistentní odkaz   https://www.medvik.cz/link/D003057
Definice

Autozomálně recesivní dědičná porucha projevující se disproporčním trpaslictvím, mikrocefalií, vpadlýma očima, zobákovitým nosem, soudkovitým hrudníkem, dermatitidou s fotosenzitivitou, hluchotou, mentální retardací a řadou dalších poruch. (cit. Velký lékařský slovník online, 2013 http://lekarske.slovniky.cz/ )

A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.

DUI
D003057 MeSH Prohlížeč
CUI
M0004689
Předchozí užití
Dwarfism (1966-1980); Photosensitivity Disorders (1966-1980)
Historická pozn.
1991(1981); use DWARFISM 1981-1990
Veřejná pozn.
1991; see DWARFISM 1981-1990

C Nemoci
C05.116 nemoci kostí 796
C05.116.099.343 nanismus 99
C05.116.099.343.110 achondroplazie 71
C05.116.099.343.250 Cockayneův syndrom 4
C05.116.099.343.347 kongenitální hypotyreóza 151
C05.116.099.343.445 hypofyzární nanismus 50
C05.116.099.343.679 Laronův syndrom 1
C05.116.099.343.796 syndrom Mulibrey 1
C05.116.099.343.957 Weillův-Marchesaniho syndrom 1
C10.574.500.024 Alexanderova nemoc 6
C10.574.500.300 syndrom Canavanové 9
C10.574.500.362 Cockayneův syndrom 4
C10.574.500.497 Huntingtonova nemoc 326
C10.574.500.529 Laforova nemoc 1
C10.574.500.545 myotonia congenita 18
C10.574.500.547 myotonická dystrofie 96
C10.574.500.549 neurofibromatózy 28
C10.574.500.850 Tourettův syndrom 86
C10.574.500.865 tuberózní skleróza 144
C16.131 vrozené vady 1 753
C16.131.077.019 syndrom delece 22q11 2
C16.131.077.065 Alagillův syndrom 19
C16.131.077.095 Angelmanův syndrom 35
C16.131.077.121 Barthův syndrom 6
C16.131.077.137 Bloomův syndrom 11
C16.131.077.229 Carneyův komplex 8
C16.131.077.245 ciliopatie 9
C16.131.077.250 Cockayneův syndrom 4
C16.131.077.256 Costellův syndrom 3
C16.131.077.272 de Langeové syndrom 4
C16.131.077.299 hluchoslepota 65
C16.131.077.313 Donohueův syndrom 1
C16.131.077.327 Downův syndrom 510
C16.131.077.350 ektodermální dysplazie 33
C16.131.077.371 Fraserův syndrom 2
C16.131.077.393 Gardnerův syndrom 21
C16.131.077.401 heterotaxe 7
C16.131.077.410 holoprosencefalie 9
C16.131.077.445 incontinentia pigmenti 19
C16.131.077.537 Loeysův-Dietzův syndrom 7
C16.131.077.550 Marfanův syndrom 105
C16.131.077.578 Moebiův syndrom 10
C16.131.077.592 moniletrichosis 1
C16.131.077.619 Nethertonův syndrom 2
C16.131.077.696 Cantrellova pentalogie 1
C16.131.077.703 POEMS syndrom 35
C16.131.077.730 Praderův-Williho syndrom 92
C16.131.077.735 nedostatek prolidázy
C16.131.077.740 Proteův syndrom 8
C16.131.077.745 prune belly syndrom 3
C16.131.077.790 zarděnky vrozené 20
C16.131.077.889 Sotosův syndrom 4
C16.131.077.919 Patauův syndrom 6
C16.131.077.929 syndrom trizomie 18 5
C16.131.077.938 Waardenburgův syndrom 10
C16.131.077.970 Zellwegerův syndrom 10
C16.320.240 nanismus 99
C16.320.240.500 achondroplazie 71
C16.320.240.562 Cockayneův syndrom 4
C16.320.240.625 kongenitální hypotyreóza 151
C16.320.240.750 Laronův syndrom 1
C16.320.240.875 syndrom Mulibrey 1
C16.320.400.024 Alexanderova nemoc 6
C16.320.400.150 syndrom Canavanové 9
C16.320.400.200 Cockayneův syndrom 4
C16.320.400.430 Huntingtonova nemoc 326
C16.320.400.480 Laforova nemoc 1
C16.320.400.540 myotonia congenita 18
C16.320.400.542 myotonická dystrofie 96
C16.320.400.550 choreoakantocytóza 6
C16.320.400.560 neurofibromatózy 28
C16.320.400.820 Tourettův syndrom 86
C16.320.400.880 tuberózní skleróza 144
C18.452 metabolické nemoci 1 200
C18.452.284 poruchy opravy DNA 10
C18.452.284.060 teleangiektatická ataxie 48
C18.452.284.100 Bloomův syndrom 11
C18.452.284.250 Cockayneův syndrom 4
C18.452.284.280 Fanconiho anemie 46
C18.452.284.520 Liův-Fraumeniho syndrom 39
C18.452.284.600 syndrom Nijmegen breakage 21
C18.452.284.960 Wernerův syndrom 14
C18.452.284.975 xeroderma pigmentosum 25

Cerebrooculofacioskeletal Syndrome 1 Disease MeSH Prohlížeč

Cerebrooculofacioskeletal Syndrome 3 Disease MeSH Prohlížeč

XFE Progeroid Syndrome Disease MeSH Prohlížeč

Xeroderma Pigmentosum B-Cockayne Syndrome Disease MeSH Prohlížeč

Xeroderma Pigmentosum, Type G-Cockayne Syndrome Disease MeSH Prohlížeč