Katarzyna Chyż
A5077431053- Metabolism and Genetic Disorders
- Diet and metabolism studies
- Mitochondrial Function and Pathology
- Neonatal Health and Biochemistry
- Amino Acid Enzymes and Metabolism
- Digestive system and related health
- Folate and B Vitamins Research
- Diet, Metabolism, and Disease
National Water Research Center
2021
Polish Mother’s Memorial Hospital Research Institute
2018
Instytut Matki i Dziecka
2018
In infants with phenylketonuria (PKU), dietary management is based on lowering and titrating phenylalanine (Phe) intake from breast milk or standard infant formula in combination a Phe-free order to maintain blood Phe levels within target range. Professionals use different methods feed PKU our survey aimed document practices across Europe.We sent cross sectional, monkey® questionnaire European health professionals working IMD. It contained 31 open multiple-choice questions. The results were...
Many countries do not have a newborn screening (NBS) program, and immigrants from such are at risk for late diagnosis of phenylketonuria (PKU). In this international survey, 52 259 patients (20%) with diagnosed PKU were immigrants, 145 the (55%) born before NBS or in location without NBS.
In phenylketonuria (PKU), weaning is considered more challenging when compared to feeding healthy infants. The primary aim of gradually replace natural protein from breast milk or standard infant formula with solids containing equivalent phenylalanine (Phe). addition, a Phe-free second stage L-amino acid supplement usually recommended around 6 months formula. Our was assess different approaches used by health professionals across Europe. A cross sectional questionnaire (survey monkey®)...
Phenylketonuria (PKU) can be effectively treated with the use of a low-phenylalanine diet. However, some patients become overweight despite proper dietary treatment. We hypothesized that this phenomenon could explained by presence specific variants within genes involved in phenylalanine transport or transamination/oxygenation pathway. selected clinically homogenous group 100 infants PKU and assessed their growth patterns context tolerance. Next, sample, we performed exome sequencing...
ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Chyż K, Hozyasz K. Comparison of diet in phenylketonuria and its costs with a traditional diet, based on 24-hour model meal plans. Pediatria Polska - Polish Journal Paediatrics. 2018;93(3):203-216. doi:10.5114/polp.2018.77434. APA Chyż, K., & Hozyasz, (2018). Paediatrics, 93(3), 203-216. https://doi.org/10.5114/polp.2018.77434 Chicago Katarzyna, Kamil Hozyasz. 2018. "Comparison plans". Paediatrics 93 (3):...
Objectives Empirical determination of phenylalanine (Phe) tolerance in patients with phenylketonuria (PKU) relies on frequent assessment blood Phe concentrations relation to intake from detailed meal records. This study aimed determine twin pregnancies. Methods The reviewed cases included three women PKU who each had a singleton and pregnancy (i.e., they were pregnant twice). All under regular supervision maintain steady state safe intake. Restriction the patient’s diet was determined...