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PJS-Pakistan Journal of Surgery. 1995; 11 (1): 55-59
en Inglés | IMEMR | ID: emr-39244

RESUMEN

Deficiency of plasma cholinesterase [ChE] was detected in several members of the family tested on suspicion of genetic modification of enzyme structure. Prolonged apnea following administration of suxamethomum [succinylecholine] was due to low levels of cholinesterase from homozygote for atypical gene [E[1a], E[1a]]. Screening of immediate relations showed atypical genetic response in cholinesterase [ChE] activity in offsprings of a heterozygous couple. [ChE [E[1a], E[1u]]. As our data are in accordance with results obtained by other investigators, this observation cannot be regarded as exceptional


Asunto(s)
Humanos , Masculino , Apnea/inducido químicamente , Colinesterasas/sangre , Succinilcolina/farmacología , Heterocigoto , Genes
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