This is the main reason why parents do not give consent

to PEG insertion for a long time and therefore feeding via nasogastric tube has to be prolonged. However, it has been proven through many studies that the impact of PEG feeding is positive and many parents reporting a high level of satisfaction [20] and wishing the procedure to be placed earlier [21]. Solely the indications for gastrostomy insertion were investigated thoroughly in this study. Other important data associated with gastrostomy in Polish children will be analyzed and published soon. The indications for gastrostomy are well established. According to our experience the main indications for pediatric gastrostomy in Polish sites were neurological disorders, especially cerebral palsy with dysphagia. Malnutrition was reported in most of children before gastrostomy placement. Endoscopic procedure was performed Selleckchem Adriamycin in most cases. More than half of investigated Palbociclib cell line patients were fed via nasogastric tube before gastrostomy placement which makes the mean time

of tube feeding prolonged regarding the actual recommendations. The decision for PEG placement should be made individually. In group of patients receiving enteral nutrition via NG the caregivers should consider PEG earlier in the decision making process. JK – study design, data collection, acceptance of final manuscript version, AW – data collection and interpretation, statistical analysis, literature search, acceptance of final manuscript version, KP, AS-S, UC-G, ET-K, BG-K, AB, MS, SW, EH – data collection, interpretation, acceptance of final manuscript version. None declared. None declared. “
“Down syndrome (DS) was first described by John Langdon Down in mid-nineteenth century. According to many authors, the most important cause of this syndrome SPTLC1 is the trisomy of the 21st chromosome [1], [2] and [3]. This notion was first presented by Lejeune et al. [4]. The trisomy of the 21st chromosome can be either mosaic or may be observed together with translocation [3] and [5]. In 95% of cases, Down syndrome originates from nondisjunction of chromosomes and in 5% of cases is associated with translocation

of 21st chromosome on one of chromosomes from group D or G. The risk of Down’s syndrome occurrence is increased when the mother’s age is more than 35 years [6]. According to Bower et al. [7], Down syndrome is the most frequently seen anomaly. Many authors give information about the prevalence rate of this syndrome. Sherman et al. [8] and [9] stated that Down syndrome was diagnosed in 1 in 732 infants in United States, whereas Irving et al. had written about the prevalence rate being 1.08 per 1000 live births in United Kingdom. According to Jamroszczyk et al., children with Down syndrome can be found in 5–10% of patients, suffering from syndromes, with boys more frequently affected than girls [10]. The mental development is considerably retarded.