hrp0084p3-851 | Fat | ESPE2015

Genotype and Clinical Characteristics in Korean Patients with Prader-Willi Syndrome: A Single Centre Study

Kim Yoo-Mi , Cheon Chong Kun , Kim Su Young

Background: Prader–Willi syndrome (PWS) is characterised by neonatal hypotonia, hypogonadism, progressive obesity, short stature, and mental retardation. This syndrome arises from a loss of expression of paternally derived genes on chromosome 15q11–13 region.Objective and hypotheses: The aim of this study was to investigate clinical characteristics and their genotypes in Korean patients with PWS.Method: The study included...

hrp0097p1-268 | Fat, Metabolism and Obesity | ESPE2023

The 2016–2021 Korea National Health and Nutrition Examination Survey for Metabolic Alteration in children and adolescent during the COVID-19 Pandemic

Kim Min-Ji , Kim Minji , Yoo Sukdong , Kun Cheon Chong

Purpose: Since the COVID-19 outbreak, the number of obese children and adolescents has increased rapidly. Obesity acts as a gateway to chronic adult diseases, so proper management during childhood and adolescence is essential. We aimed to identify the interannual changes in the prevalence of obesity, diabetes mellitus, dyslipidemia, and hypertension, and to investigate factors contributing to these changes before and during the COVID-19 pandemic.<p class="...

hrp0097p1-527 | Growth and Syndromes | ESPE2023

Application of next-generation sequencing in patients suspected of having skeletal dysplasia

Kim Minji , Kim Min-Ji , Kun Cheon Chong

Background: Skeletal dysplasias (SD) are a heterogeneous group of heritable conditions with generalized bone and cartilage impairment caused by pathogenic variants in genes primarily affecting skeletogenesis and/or bone homeostasis. In this study, we conducted a next-generation sequencing (NGS) in patients with a suspected SD to reveal the underlying etiologies of skeletal dysplasia.Methods: Thirty-four pediatric patient...

hrp0097p2-9 | Growth and Syndromes | ESPE2023

A novel COL11A1 gene mutation in a patient with short stature mimicking Noonan syndrome

Kim Minji , Kim Min-Ji , Kun Cheon Chong

Background: Fibrochondrogenesis 1 (FBCG1) is known as an autosomal recessive syndrome, which is related to short-limbed skeletal dysplasia. The disease is clinically characterized by a flat midface with a small nose and anteverted nares, significant shortening of all limb segments but relatively normal hands and feet, and a small bell-shaped thorax with a protuberant abdomen. Mutations in the gene encoding the α1 chain of type XI collagen (COL11A1) are s...

hrp0092p1-349 | Fat, Metabolism and Obesity (2) | ESPE2019

Prevalence of Dyslipidemia in Korean Youth Over 10 Years: Data from the Korea National Health and Nutrition Examination Survey 2008-2017

Lee Jieun , Kim Jae Hyun

Objectives: Dyslipidemia begins and continues in youth and is a major risk factor for adult-onset cardiovascular disease. The aim of this study was to investigate the prevalence and trend of dyslipidemia in Korean youth and its trends for 10 years.Methods: Study subjects were Korean youth aged 10-18 years who participated in the Korea National Health and Nutrition Examination Survey (KNHANES). A total of 7,466 eligible p...

hrp0089p2-p046 | Bone, Growth Plate &amp; Mineral Metabolism P2 | ESPE2018

Novel SLC34A1 Mutation in a Girl Infant with Idiopathic Infantile Hypercalcemia

Kang Seokjin , Kim Heung Sik

SLC34A1 encodes renal sodium-phosphate cotransporter 2A. It has been identified as being a part of the etiology of idiopathic infantile hypercalcemia. We report a case of a 1-month old girl, initially hospitalized due to perinatal detection of nephrocalcinosis. Blood tests showed hypercalcemia, hypophosphatemia, hypercalciuria and increased 1,25-(OH)2D3. Renal ultrasound revealed medullary nephrocalcinosis. An abnormality in vitamin-D metabolism was suspected and genetic testi...

hrp0089p2-p083 | Diabetes &amp; Insulin P2 | ESPE2018

Relation between Hypomagnesemia and Increased Level of HbA1c in Patients with Diabetes Mellitus

Kang Seokjin , Kim Heung Sik

Background: Hypomagnesemia is a frequent condition in patients with diabetes mellitus (DM). It could influence metabolic control in patients with DM. Relevant studies concern mainly adults and there are few data from the pediatric population. The aim of the present study was to evaluate magnesium levels and examine their possible association with glycemic control in pediatric patients with diabetes mellitus.Methods: In all, 36 patients with DM (type 1, 3...

hrp0086p2-p520 | Fat Metabolism and Obesity P2 | ESPE2016

Preliminary Findings on Nutrition Care Competence in Health Care Professionals Using a Standardized Questionnaire NUTCOMP Korean Version

Kim Kieun , Kim Gyeong-Mi , Jeong Mi-Yong , Kim Yanghyeon , Lee Kyu-Rae , Kim Sun-Hyeon , Baik Seolhyang , Shin Hyejeong

Background: It is well known that obesity, diabetes or chronic disease are related with nutrition. However it has not been known whether health providers have concepts or competence about counseling of nutritional support in clinical practice basis. There is rare of information about differences among types of profession jobs.Objective and hypotheses: We investigated a survey with standardized questionnaire tool among different types of profession jobs d...

hrp0084p3-709 | Diabetes | ESPE2015

Elevated HbA1c and Cardiometabolic Risk Factors in Korean Children and Adolescents: Data from the Korean National Health and Nutrition Examination Survey, 2011–2012

Lee Jieun , Kim Jae Hyun

Background: Prediabetes often precedes type 2 diabetes, which is associated with obesity and increased risk of developing cardiovascular disease. Haemoglobin A1c (HbA1c) has been recently recommended as a useful tool for the diagnosis of diabetes and prediabetes.Objective and hypotheses: We investigated whether prediabetes according to HbA1c was associated with cardiometabolic risk factors in Korean children and adolescents.Method:...

hrp0084p3-1154 | Puberty | ESPE2015

The Relationships between Serum Vitamin D Level and Precocious Puberty in Korean Girls

Kim Se Young , Woo Yeoloon

Background: The recent articles showed a kind of associations of the serum vitamin D levels and chronic diseases, for example, autoimmune diseases, vascular disorders, as well as malignancies. Also vitamin D deficiency impacts normal growth and maximal bone mineral accretion in puberty. Of pediatric population in Korea, the prevalence of cases of vitamin D deficiency and precocious puberty were continuously increasing nowadays.Objective and hypotheses: W...