nemoc z nedostatku ornithinkarbamoyltransferázy [Ornithine Carbamoyltransferase Deficiency Disease]

tematický
19
Termíny

deficit ornitintranskarbamoylázy
deficit OTC
ornithinkarbamoyltransferasa - nedostatek
ornithintranskarbamylasa - nedostatek

 

Deficiency Disease, Ornithine Carbamoyltransferase
Deficiency Disease, Ornithine Transcarbamylase
Ornithine Carbamoyltransferase Deficiency
Ornithine Transcarbamylase Deficiency
Ornithine Transcarbamylase Deficiency Disease
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To
OTC Deficiency

Perzistentní odkaz   https://www.medvik.cz/link/D020163
Definice

Vrozená porucha metabolismu ornithinu (v močovinovém cyklu) s vazbou na X chromozom. Klinicky se projevuje atakami hyperamonemie (zvracení, neurologická symptomatologie vč. kómatu), nejč. po převedení kojence na potravu s vysokým obsahem proteinů. Opakované ataky vedou k psychomotorické retardaci. Včasná diagnostika s transplantací jater je jediná kauzální, úspěšná léčba u řady těchto pacientů. (cit. Velký lékařský slovník online, 2015 http://lekarske.slovniky.cz/ )

An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)

DUI
D020163 MeSH Prohlížeč
CUI
M0328321
Předchozí užití
Ornithine Carbamoyltransferase/deficiency (1966-1999)
Historická pozn.
2000
Veřejná pozn.
2000

C Nemoci
C10.228.140 nemoci mozku 1 177
C10.228.140.163 metabolické nemoci mozku 84
C10.228.140.163.100.937 vrozené poruchy cyklu močoviny 7
C10.228.140.163.100.937.124 argininjantarová acidurie 2
C10.228.140.163.100.937.374 citrulinemie 2
C10.228.140.163.100.937.500 hyperargininemie 2
C16.320.322.030 Aicardiho syndrom
C16.320.322.068 Barthův syndrom 6
C16.320.322.092 choroideremie 3
C16.320.322.100 Dentova choroba 1
C16.320.322.108 dyskeratosis congenita 9
C16.320.322.124 Fabryho nemoc 187
C16.320.322.201 glykogenóza typu IIb 11
C16.320.322.217 glykogenóza typu VIII
C16.320.322.235 hemofilie B 214
C16.320.565.100.940.124 argininjantarová acidurie 2
C16.320.565.100.940.374 citrulinemie 2
C16.320.565.100.940.500 hyperargininemie 2
C16.320.565.189.937.124 argininjantarová acidurie 2
C16.320.565.189.937.374 citrulinemie 2
C16.320.565.189.937.500 hyperargininemie 2
C18.452 metabolické nemoci 1 196
C18.452.132.100.937.124 argininjantarová acidurie 2
C18.452.132.100.937.374 citrulinemie 2
C18.452.132.100.937.437 hyperargininemie 2
C18.452.648.100.940.124 argininjantarová acidurie 2
C18.452.648.100.940.374 citrulinemie 2
C18.452.648.100.940.437 hyperargininemie 2
C18.452.648.189.937.124 argininjantarová acidurie 2
C18.452.648.189.937.374 citrulinemie 2
C18.452.648.189.937.437 hyperargininemie 2