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...

hrp0082p2-d2-302 | Bone (1) | ESPE2014

Plasma 25-OH Vitamin D and pth Concentrations in Cord Blood: relationship with Ethnic Groups, Nutritional Habits and Degree of Maternal Sun Exposure

Ortigosa Gomez Sandra , Garcia Algar Oscar , Mur Sierra Antonio , Ferrer Costa Roser , Carrascosa Lezcano Antonio , Yeste Fernandez Diego

Introduction: Several studies showing a high prevalence of vitamin D deficiency in pregnant women have been published in recent years. Vitamin D deficiency during pregnancy has been related to adverse events both in mother and child. Plasma 25-OH vitamin D (25(OH)D) levels in the newborn are dependent on maternal deposits and show a close correlation with maternal levels; thus, neonates of vitamin D-deficient mothers present a greater risk of hypocalcaemia, rickets and a highe...

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...

hrp0082p3-d3-732 | Diabetes (2) | ESPE2014

The Pattern of Body Composition Change in Type 1 Diabetes by Gender

Kim Yong Hyuk , Park Hye Won , Kim Kyo Sun , Chung Sochung

Background: Childhood period is associated with growth accompanied by rapid change of body composition. Excessive fat gain and followed increased insulin resistance is an obstacle in controlling blood sugar for type 1 diabetic patients.Objective and hypotheses: This study was designed to understand the gender difference in the patterns of body composition change along the growth process of newly diagnosed type I diabetic children and adolescents.<p c...

hrp0084p2-513 | Pituitary | ESPE2015

A Novel Mutation within the AVP Gene in an 18-Year-Old Male Patient with Kallmann Syndrome and Combined Pituitary Hormone Deficiency

Choi Won Bok , Kim Soo Young , Yoon Lira , Kim Young Mi , Cho Min-Jung , Ki Chang-Seok , Cho Sung Yoon , Jin Dong-Kyu , Kwak Min Jung

Background: Kallmann syndrome is the most common form of hypogonadotropic hypogonadism and is associated with genes such as KAL1, KAL2, CHD7, NELF, PROK2, and PROKR2. Genetic factors in hypopituitarism are involved with the gene mutation of PROP1, POU1F1, HESX1, LHX3, LHX4, and PTX2. We found a novel mutation of the AVP gene in a Kallmann syndrome patient with hypopituitarism.Case presentation: The pa...

hrp0097p1-348 | Pituitary, Neuroendocrinology and Puberty | ESPE2023

Clinical course and genetic analysis in patients with childhood-onset congenital combined pituitary hormone deficiency

Ha Lee Yoon , Young Kim Ka , Hye Lee Da , Jee Kim Min , Jeong Lee Yun , Ah Lee Young , Min Ko Jung , Ho Shin Choong

Background: Congenital combined pituitary hormone deficiency (CPHD) has various clinical presentations and can be caused by genetic defects related to pituitary development. We investigated the clinical features and genetic analysis in Korean patients with congenital CPHD.Method: Among 444 patients diagnosed with CPHD between 1994 and 2021 from Seoul National University Children’s Hospital, 43 patients with congeni...

hrp0082p1-d2-210 | Reproduction (1) | ESPE2014

Messenger Ribonucleic Acid Expression of Kiss-1 and Serum Level of Kisspeptin in Rat at Different Developmental Stages

Reum Kwon Ah , Hee Kim Duk , Min Ahn Jung , Song Kyungchul , Wook Chae Hyun , Kim Ho-Seong , Jin Kim Ye , Hyuk Kim Yong

Background: KiSS-1 and its product, kisspeptin is necessary for puberty onset and proper adult gonadal function due to its stimulatory effect on the secretion of gonadotropin-releasing hormone (GnRH). Although the pathophysiological importance of KiSS-1 and kisspeptin is well known, the developmental patterns of expression of KiSS-1 genes and serum level of kisspeptin have not been explored to date.Objective and hypotheses: We report herein the expressio...

hrp0082p3-d2-673 | Bone (1) | ESPE2014

Normal Bone Mineral Acquisition in Korean Adolescents; Korea National Health and Nutrition Examination Surveys

Park Hye Won , Kwak Byung Ok , Kim Kyo Sun , Chung Sochung

Background: The large portion of bone mass is acquired with body growth during adolescent period and peak bone mass is achieved in early adulthood. Body composition is known as predictor of bone health.Objective and hypotheses: The aims of this study were to evaluate normal bone mineral acquisition during adolescent period and to determine the factor that affects on it in Korean.Method: This study was based on data from the Fourth ...