hrp0082p1-d2-80 | Diabetes (1) | ESPE2014

Methylmalonic Acidemia (MMA) with Unusual Presentation Mimicking Diabetic Ketoacidosis

Dejkhamron Prapai , Wejaphikul Karn , Katanyuwong Kamornwan , Unachak Kevalee , Wattanasirichaigoon Duangrurdee , Tanpaiboon Pranoot

Background: Hyperglycemic ketoacidosis is an acute, life threatening condition requiring early etiologic recognition and management to prevent serious morbidity/mortality. The most common cause is diabetic ketoacidosis (DKA). Organic acidaemias (OAs) are inheritable metabolic disorders caused by defects in protein metabolism resulting in acid accumulation. Patients with metabolic decompensation usually present with lactic and/or ketoacidosis, with/without hypoglycemia. Hypergl...

hrp0097p1-36 | Diabetes and Insulin | ESPE2023

Incidence of Newly Diagnosed Childhood Diabetes and Severity at Onset Between Pre-Pandemic and Pandemic COVID-19 Eras in Northern Thailand

Sinthuprasith Pattharaporn , Wejaphikul Karn , Puttawong Dolrutai , Tang-Ngam Hataitip , Sanrattana Naphatsorn , Unachak Kevalee , Dejkhamron Prapai

Background: The incidence rate (IR) of childhood diabetes is increasing globally. These upward trends were also found in Thailand. However, newly diagnosed childhood diabetes incidences are not updated, especially in Northern Thailand. There are possibilities that COVID-19 pandemic affects the development of acute diabetes after infection and the severity of the first clinical presentation of childhood diabetes. However, data are also conflicting regarding the...

hrp0097p1-591 | Thyroid | ESPE2023

Health-Related Quality of Life in Patients Diagnosed with Childhood Primary Hyperthyroidism

Pitupan Pakanut , Dejkhamron Prapai , Boonchooduang Nonglak , Puttawong Dolrutai , Wongsa Danil , Unachak Kevalee , Wejaphikul Karn

Background: Hyperthyroidism is a common condition in general pediatric practice. Several adult studies show hyperthyroidism affects health-related quality of life (HRQoL). However, information regarding HRQoL in the pediatric population is limited.Objectives: To evaluate HRQoL and psychosocial functioning of patients diagnosed with childhood primary hyperthyroidism compared with healthy controls and to identify the possi...

hrp0097p2-171 | Bone, Growth Plate and Mineral Metabolism | ESPE2023

An Infantile Hypophosphatasia with Novel Mutation in ALPL Gene: A Case Report

Wejaphikul Karn , Sinthuprasith Pattharaphorn , Fanhchaksai Kanda , Kangsuwan Supakanya , Damrongmanee Alisara , Kittisakmontri Kulnipa , Puttawong Dolrutai , Unachak Kevalee , Dejkhamron Prapai

Background: Hypophosphatasia (HPP) is a rare inherited disease of bone metabolism caused by inactivating mutations in the ALPL gene encoding tissue non-specific alkaline phosphatase (TNSAP). Infantile HPP is characterized by early onset abnormal skeletal mineralization with hypercalcemia and low alkaline phosphatase (ALP). It has been rarely reported from Thailand, resulting in limited disease awareness. We reported an infantile HPP Thai patient who p...