Relapsing Infection in an Infant with Intermittent Stridor
Recidivující infekce u kojence s intermitentním stridorem
Autoři uvádějí kazuistiku 4měsíčního kojence s recidivujícími infekty, jejichž příčinou byl atypicky utvářenýaortální oblouk.
Klíčová slova:
recidivující infekce, zdvojený aortální oblouk
Authors:
K. Bajerová; M. Bajer
Authors‘ workplace:
I. dětská interní a onkologická klinika, FN Brno - Dětská nemocnice J. G. Mendela, přednostka doc. MUDr. H. Hrstková, CSc.
Published in:
Čes-slov Pediat 1999; (8): 431-432.
Category:
Overview
The authors present a case of an infant with recurrent infections of the respiratory tract, which resulted froman atypical aortic arch.
Key words:
recurrent infections, double aortic arch
Labels
Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
1999 Issue 8
- What Effect Can Be Expected from Limosilactobacillus reuteri in Mucositis and Peri-Implantitis?
- The Importance of Limosilactobacillus reuteri in Administration to Diabetics with Gingivitis
-
All articles in this issue
- Autosomal Recessive and Dominant Polycystic Kidney Disease
- New Face of Smith-Lemli-Opitz Syndrome
- Mutation Analysis of COL4A5 and COL4A3 Genes in Alport’s Syndrome
- Fate of Children with Endocardial Fibroelastosis in Adult Age
- Development of Parameters of Heart Rate Variability in Young Subjects Aged 15 - 19 Years
- Frequency of Bacterial Pathogens and their Resistance to Antimicrobial Drugs at the PaediatricClinic, Faculty Hospital Olomouc
- Relapsing Infection in an Infant with Intermittent Stridor
- Electroconvulsive Therapy: An Effective Method for Treatment of Adolescent Psychoses
- PEHO Syndrome
- Incidence of Birth Defects and Successful Prenatal Diagnosis in the Czech Republic in 1997
- Czech-Slovak Pediatrics
- Journal archive
- Current issue
- About the journal
Most read in this issue
- New Face of Smith-Lemli-Opitz Syndrome
- Autosomal Recessive and Dominant Polycystic Kidney Disease
- Mutation Analysis of COL4A5 and COL4A3 Genes in Alport’s Syndrome
- Fate of Children with Endocardial Fibroelastosis in Adult Age