Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Korean Journal of Pediatric Gastroenterology and Nutrition ; : S1-S9, 2010.
Article in Korean | WPRIM | ID: wpr-219038

ABSTRACT

Infancy and childhood are marked by rapid physical growth and development, and infant's and child's health and development depends on good nutrition. Any disruption in appropriate nutrient intake may have lasting effects on growth potential and development achievement. Nutrition needs and feeding patterns vary significantly in each stage of growth and development. This article summarized the key nutritional issues in the Korea national health screening program for infants and children as followings: encouraging breastfeeding, healthier complementary feeding, healthy foods selection, healthy eating habits, coping with feeding problem (picky eating), and overweight prevention with an emphasis on physical activity.


Subject(s)
Child , Humans , Infant , Achievement , Breast Feeding , Eating , Feeding Behavior , Growth and Development , Infant Nutritional Physiological Phenomena , Korea , Mass Screening , Motor Activity , Overweight
2.
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 179-186, 2008.
Article in Korean | WPRIM | ID: wpr-106811

ABSTRACT

PURPOSE: Feeding problems are common for typically developing children and have negative effects on physical, behavioral, and cognitive development. The purpose of the current study was to examine factors related to childhood feeding problems for typically developing children via parental reports. METHODS: The feeding questionnaire developed by the authors and the Childhood Eating Behavior Inventory (CEBI) were administered to 796 parents of children who recruited from 2 pediatric outpatient clinics (n=379) and community (n=417). Problem eaters (PE) were identified by parental report and frequency analysis was conducted for types of feeding problems and its severity, problem behaviors during mealtime, the feeding methods of the parents, and the need for treatment. RESULTS: The CEBI scores were significantly different between the PE and non-problem eaters (NPE), which suggests that the parental reports were reliable. The younger children had more feeding problems than the older children. The most frequent and severe feeding problems were selective eating and longer mealtimes across all age groups. One-half of the children had more than one problem behaviors during mealtime. Most parents of PE used ineffective methods to deal with children's behaviors during meal time, such as cajoling, which was related to their increased level of stress. Many parents reported their children need professional help for the feeding problems. CONCLUSION: Feeding problems are prevalent among children, especially younger children. Children with feeding problems showed a number of problem behaviors during mealtime and parental coping methods appeared to be ineffective. The need for treatment was considerable, thus the characteristics of this population must be acknowledged for providing proper treatment and advice.


Subject(s)
Child , Humans , Ambulatory Care Facilities , Eating , Feeding Behavior , Feeding Methods , Meals , Parents , Surveys and Questionnaires
3.
Journal of the Korean Pediatric Society ; : 1142-1148, 2000.
Article in Korean | WPRIM | ID: wpr-154006

ABSTRACT

Prader-Willi syndrome(PWS) was first described by Prader et al in 1956. This syndrome is characterized by diminished fetal activity, low birth weight, infantile hypotonia with feeding problem, temperature instability, early onset of childhood hyperphagia with consequent obesity, short stature, hypogonadism and mental retardation. The deletion of chromosome 15(del 15(qll-13)) was reported by Ledbetter in 1981, which was thought to be of paternal origin. Recently, such micro- deletion may be diagnosed by fluorescence in situ hybridization(FISH) that recognizes specific DNA base sequence. We experienced a Prader-Willi syndrome confirmed by FISH in an infant that had hypotonia, growth retardation, feeding difficulty and FUO since 1 month of age. We report this case with a brief review and related literature.


Subject(s)
Humans , Infant , Infant, Newborn , Base Sequence , DNA , Fetal Movement , Fluorescence , Hyperphagia , Hypogonadism , Infant, Low Birth Weight , Intellectual Disability , Muscle Hypotonia , Obesity , Prader-Willi Syndrome
SELECTION OF CITATIONS
SEARCH DETAIL