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syndrom kočičího mňoukání [Cri-du-Chat Syndrome]

tematický
11
Termíny

cri-du-chat syndrom
syndrom cri du chat
syndrom kočičího křiku

 

5p Deletion Syndrome
5p Minus Syndrome
5p- Syndrome
Cat Cry Syndrome
Chromosome 5 Short Arm Deletion Syndrome
Chromosome 5p Deletion Syndrome
Chromosome 5p- Syndrome
Crying Cat Syndrome
Deletion of Short Arm of Chromosome 5 Syndrome

Perzistentní odkaz   https://www.medvik.cz/link/D003410
Definice

Syndrom nazván podle typického pláče postiženého novorozence. Je způsoben delecí krátkého raménka 5. chromozomu a vyznačuje se mentální retardací, mikrocefalií, antimongoloidním sklonem očí a srdečními vadami. (cit. Velký lékařský slovník online, 2012 http://lekarske.slovniky.cz/ )

An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-).

DUI
D003410 MeSH Prohlížeč
CUI
M0005309
Historická pozn.
1977; use CRYING CAT SYNDROME 1964-1976
Veřejná pozn.
1977; see CRYING CAT SYNDROME 1964-1976

C Nemoci
C10.597.606.360 mentální retardace 1 060
C10.597.606.360.180 syndrom kočičího mňoukání 11
C10.597.606.360.210 de Langeové syndrom 4
C10.597.606.360.220 Downův syndrom 511
C10.597.606.360.690 Praderův-Williho syndrom 94
C10.597.606.360.700 Rubinsteinův-Taybiho syndrom 12
C10.597.606.360.835 Patauův syndrom 6
C10.597.606.360.969 syndrom WAGR 3
C10.597.606.360.970 Williamsův-Beurenův syndrom 22
C16.131 vrozené vady 1 758
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 511
C16.131.077.350 ektodermální dysplazie 34
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 2
C16.131.077.703 POEMS syndrom 35
C16.131.077.730 Praderův-Williho syndrom 94
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
C16.131.260.019 syndrom delece 22q11 2
C16.131.260.040 Angelmanův syndrom 35
C16.131.260.210 de Langeové syndrom 4
C16.131.260.260 Downův syndrom 511
C16.131.260.380 holoprosencefalie 9
C16.131.260.440 Jacobsenův syndrom 1
C16.131.260.700 Praderův-Williho syndrom 94
C16.131.260.905 Sotosův syndrom 4
C16.131.260.923 Patauův syndrom 6
C16.131.260.932 syndrom trizomie 18 5
C16.131.260.940 syndrom WAGR 3
C16.320.180.019 syndrom delece 22q11 2
C16.320.180.040 Angelmanův syndrom 35
C16.320.180.210 de Langeové syndrom 4
C16.320.180.260 Downův syndrom 511
C16.320.180.380 holoprosencefalie 9
C16.320.180.440 Jacobsenův syndrom 1
C16.320.180.700 Praderův-Williho syndrom 94
C16.320.180.905 Sotosův syndrom 4
C16.320.180.923 Patauův syndrom 6
C16.320.180.932 syndrom trizomie 18 5
C16.320.180.940 syndrom WAGR 3

Chromosome 5, monosomy 5q35 Disease MeSH Prohlížeč

Chromosome 5, trisomy 5p Disease MeSH Prohlížeč

Chromosome 5, trisomy 5pter p13 3 Disease MeSH Prohlížeč

Chromosome 5, trisomy 5q Disease MeSH Prohlížeč

Chromosome 5, uniparental disomy Disease MeSH Prohlížeč

Monosomy 5p Disease MeSH Prohlížeč