Authors: L. Žídková 1; M. Procházka 2; A. Šantavá 3; T. Adam 1 Authors‘ workplace: Laboratoř dědičných metabolických poruch, Oddělení klinické biochemie FN, Olomouc přednosta doc. MUDr. P. Schneiderka, CSc. 1; Porodnicko-gynekologická klinika LF UP, Olomouc, přednosta prof. MUDr. M. Kudela, CSc. 2; Ústav lékařské genetiky a fetální medicíny, FN a LF UP, Olomouc přednosta prof. MUDr. J. Šantavý, CSc. 3 Published in: Ceska Gynekol 2007; 72(5): 316-320 Category: Original Article
Objective: Review of contemporary knowledge about inherited metabolic disorders in pregnant women and fetuses.
Design: A review of literature.
Setting: Laboratory for inherited metabolic disorders, Departament of Clinical Biochemistry and Childern’s Clinic, University Hospital and Palacky University, Olomouc.
Method: Review of literature and publications using medical databases.
Conclusion: Metabolic examination of mother or child is recommended if any clinical problems during or immediately after pregnancy occur. Nowadays most of inherited errors of metabolism can be diagnosed prenataly in first or second trimester of pregnancy.
Key words: inherited disorders of metabolism, prenatal diagnosis, pregnancy, abortions, HELLP syndrome, AFLP syndrome
Don‘t have an account? Create new account
Enter the email address that you registered with. We will send you instructions on how to set a new password.
