HYPOGLYCEMIA IN INFANTS AND CHILDREN

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。本项目的具体目标是：1。目的：对婴幼儿低血糖相关疾病进行临床诊断和分类；2. 为低血糖相关疾病患者的分子遗传分析提供遗传物质（DNA和系谱信息）；3. 提供一个论坛，开展旨在了解低血糖产生障碍儿童的自然历史的研究，特别是那些患有高胰岛素症、脂肪酸氧化或运输缺陷和糖原储存疾病的儿童；4. 提供论坛，教授研究员、住院医师和医学生关于婴儿和儿童低血糖及其相关疾病的诊断和管理。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The specific aims of this project are: 1. to clinically diagnose and classify disorders associated with hypoglycemia in infants and chilren; 2. to provide the genetic material (DNA and pedigree information) for molecular genetic analysis from subjects with defined disorders associated with hypoglycemia; 3. to profice a forum in which to perform studies aimed at understanding the natural history of children with hypoglycemia-producing disorders, especially those with hyperinsulinism, defects in fatty acid oxidation or transport, and glycogen storage diseases; 4. to provide the forum in which to teach fellows, residents, and medical students about the diagnosis and management of infants and children with hypoglycemia and its related disorders.