26 results match your criteria: "Sowha Children's Hospital[Affiliation]"

Background: The diagnosis of pediatric acute respiratory distress syndrome (PARDS) is a pragmatic decision based on the degree of hypoxia at the time of onset. We aimed to determine whether reclassification using oxygenation metrics 24 hours after diagnosis could provide prognostic ability for outcomes in PARDS.

Methods: Two hundred and eighty-eight pediatric patients admitted between January 1, 2010 and January 30, 2017, who met the inclusion criteria for PARDS were retrospectively analyzed.

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Article Synopsis
  • Bronchiectasis is a chronic lung disease in children marked by irreversible airway dilation, with a study focusing on its causes and features in Korean kids from 2000 to 2017.
  • Out of 387 cases, children were diagnosed at an average age of 9.2 years, predominantly boys, with respiratory infections being the leading cause (55.3%).
  • The study highlights common symptoms like chronic cough and recurrent pneumonia, emphasizing the need for further research to improve management and outcomes for these patients.
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Incidence and Prevalence of Central Precocious Puberty in Korea: An Epidemiologic Study Based on a National Database.

J Pediatr

May 2019

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea. Electronic address:

Article Synopsis
  • The study aimed to analyze the rates of central precocious puberty in Korea using health insurance claims data from 2008 to 2014.
  • A total of 37,890 girls and 1,220 boys were diagnosed, revealing an incidence rate of 122.8 per 100,000, significantly higher in girls (262.8) compared to boys (7.0).
  • Findings indicated a steep rise in both the incidence and prevalence of central precocious puberty during the study period, highlighting the need for further research into its causes.
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Background: Test for Respiratory and Asthma Control in Kids (TRACK) questionnaires were developed and validated in various languages to monitor respiratory control in preschool-aged children. We aimed to assess the reliability and validity of the Korean version of the TRACK questionnaire.

Methods: We administered the linguistically validated TRACK questionnaires to caregivers of asthmatic preschool children on two separate visits 4-6 weeks apart.

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Purpose: Cockroach exposure is a pivotal cause of asthma. Tight junctions are intercellular structures required for maintenance of the barrier function of the airway epithelium, which is impaired in this disease. Matrix metalloproteinases (MMPs) digest extracellular matrix components and are involved in asthma pathogenesis: MMP1 is a collagenase with a direct influence on airway obstruction in asthmatics.

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Respiratory failure in a diabetic ketoacidosis patient with severe hypophosphatemia.

Ann Pediatr Endocrinol Metab

June 2018

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Article Synopsis
  • Phosphate is crucial for human metabolism, and severe hypophosphatemia can lead to serious health issues like neurologic and cardiac problems.
  • A 14-year-old girl with type 1 diabetes experienced DKA treatment complications, including seizures and cardiac arrest, but stabilized after resuscitation.
  • After developing respiratory failure due to low phosphate levels, she recovered fully once the hypophosphatemia was treated, highlighting the need for careful phosphate monitoring in DKA patients.
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A boy with 46,X,+mar presenting gynecomastia and short stature.

Ann Pediatr Endocrinol Metab

December 2017

Division of Pediatric Endocrinology, Department of Pediatrics, Endocrine Research Institute, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.

A 15-year-old boy was referred due to gynecomastia and short stature. He was overweight and showed the knuckle-dimple sign on the left hand, a short fourth toe on the left foot, and male external genitalia with a small phallus. His levels of estradiol and follicle-stimulating hormone were increased, and his testosterone concentration was normal.

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Article Synopsis
  • This study investigates the role of serum albumin as a predictor of disease severity and mortality in pediatric ICU patients, contrasting it with other existing mortality indices.
  • It analyzed medical records from 431 children admitted to the ICU, excluding those with certain conditions or early deaths, to assess albumin levels and their correlation with mortality rates and other health indicators.
  • Findings indicate that children with low serum albumin (hypoalbuminemia) have significantly higher mortality rates and poorer health outcomes, suggesting it could serve as an important biomarker for poor prognosis in critically ill children.
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Purpose: Precocious puberty has significantly increased recently. While obesity is associated with puberty timing, the relationship between obesity and central precocious puberty (CPP) remains controversial. The purpose of this study was to determine whether insulin resistance is associated with bone age (BA) advancement in girls with CPP.

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Clinical manifestations of Rathke's cleft cysts and their natural progression during 2 years in children and adolescents.

Ann Pediatr Endocrinol Metab

September 2017

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Purpose: Rathke's cleft cyst (RCC) is an asymptomatic benign lesion. With increased interest in pediatric endocrinology, the prevalence of RCCs in children is also increasing. However, the clinical relevance and proper management of RCC is not well defined in children.

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Diabetes mellitus due to agenesis of the dorsal pancreas in a patient with heterotaxy syndrome.

Ann Pediatr Endocrinol Metab

June 2017

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Article Synopsis
  • Heterotaxy syndrome (HS) is a congenital disorder characterized by the abnormal placement of internal organs, often associated with cardiovascular and digestive system defects.
  • A case study discusses a 13-year-old girl who developed diabetes mellitus due to dorsal pancreatic agenesis, along with HS manifesting as a double-outlet right ventricle, pulmonary stenosis, and intestinal malrotation.
  • The girl's condition was effectively managed with timely diagnosis and insulin treatment, leading to improved blood sugar control.
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Article Synopsis
  • Chylomicronemia is a serious condition resulting from a genetic defect in the breakdown of fats, leading to dangerously high triglyceride levels and potential complications like pancreatitis.
  • A one-month-old infant was diagnosed incidentally with this condition during a hospital stay, showing extremely high triglyceride levels (>5,000 mg/dL) and required urgent treatment through plasmapheresis.
  • Genetic testing identified a new mutation associated with the condition, and the infant's triglyceride levels have stabilized with no rebound issues post-treatment.
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Risk of Gonadoblastoma Development in Patients with Turner Syndrome with Cryptic Y Chromosome Material.

Horm Cancer

June 2017

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, South Korea.

Current guidelines recommend that testing for Y chromosome material should be performed only in patients with Turner syndrome harboring a marker chromosome and exhibiting virilization in order to detect individuals who are at high risk of gonadoblastoma. However, cryptic Y chromosome material is suggested to be a risk factor for gonadoblastoma in patients with Turner syndrome. Here, we aimed to estimate the frequency of cryptic Y chromosome material in patients with Turner syndrome and determine whether Y chromosome material increased the risk for development of gonadoblastoma.

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Purpose: Abdominal obesity is a fundamental factor underlying the development of metabolic syndrome. Because of radiation exposure and cost, computed tomography or dual-energy X-ray absorptiometry to evaluate abdominal adiposity are not appropriate in children. Authors evaluated whether ultrasound results could be an indicator of insulin resistance and nonalcoholic fatty liver disease (NAFLD).

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Male patients presenting with rapidly progressive puberty associated with malignant tumors.

Ann Pediatr Endocrinol Metab

March 2016

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

In males, precocious puberty (PP) is defined as the development of secondary sexual characteristics before age 9 years. PP is usually idiopathic; though, organic abnormalities including tumors are more frequently found in male patients with PP. However, advanced puberty in male also can be an important clinical manifestation in tumors.

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A 14-year-old girl was referred for evaluation of the etiology of Cushing syndrome. During the previous 2 years, she had experienced weight gain, secondary amenorrhea, growth retardation, and back pain. Random serum cortisol level, 24-hour urinary free cortisol excretion, and overnight and low-dose dexamethasone suppression tests suggested Cushing syndrome.

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XYY syndrome: a 13-year-old boy with tall stature.

Ann Pediatr Endocrinol Metab

September 2015

Department of Pediatrics, Severance Children's Hospital, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

When evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess growth hormone secretion, Marfan syndrome, androgen or estrogen deficiency, testicular feminization, and sex chromosome anomaly, such as Klinefelter syndrome and XYY syndrome. Men with 47,XYY syndrome can exhibit multiple phenotypes.

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Hypotonic hyponatremia by primary polydipsia caused brain death in a 10-year-old boy.

Ann Pediatr Endocrinol Metab

September 2015

Department of Pediatrics, Severance Children's Hospital, Institute of Endocrinology, Yonsei University College of Medicine, Seoul, Korea.

Hypotonic hyponatremia by primary polydipsia can cause severe neurologic complications due to cerebral edema. A 10-year-and-4-month-old boy with a psychiatric history of intellectual disability and behavioral disorders who presented with chief complaints of seizure and mental change showed severe hypotonic hyponatremia with low urine osmolality (serum sodium, 101 mmol/L; serum osmolality, 215 mOsm/kg; urine osmolality, 108 mOsm/kg). The patient had been polydipsic for a few months prior, and this had been worse in the previous few days.

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Purpose: Previous studies have revealed many inconsistent results regarding the relationship between vitamin D and metabolic syndrome. The purpose of our study was to investigate the association between serum 25-hydroxyvitamin D (25(OH)D) concentration and factors that characterize metabolic syndrome in Korean children and adolescents.

Methods: We analyzed data from 2,880 children and adolescents aged 10-18 years collected from the 2008-2010 Korean National Health and Nutrition Examination Survey.

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Purpose: Although microalbuminuria is considered as an early marker of nephropathy in diabetic adults, available information in diabetic adolescents is limited. The aim of this study was to investigate prevalence and frequency of regression of microalbuminuria in type 1 (T1DM) and type 2 diabetes mellitus (T2DM) patients with childhood onset.

Methods: One hundred and nine adolescents (median, 18.

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Growth hormone treatment and risk of malignancy.

Korean J Pediatr

February 2015

Department of Pediatrics, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Growth hormone (GH) treatment has been increasingly widely used for children with GH deficiencies as the survival rate of pediatric patients with malignancies has increased. Both GH and insulin-like growth factor-I have mitogenic and antiapoptotic activity, prompting concern that GH treatment may be associated with tumor development. In this review, the authors examined the relationship between GH treatment and cancer risk in terms of de novo malignancy, recurrence, and secondary neoplasm.

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Purpose: There is controversy surrounding the growth outcomes of treatment with gonadotropin-releasing hormone agonist (GnRHa) in central precocious puberty (CPP). We analyzed height preservation after treatment with GnRHa with and without growth hormone (GH) in girls with CPP.

Methods: We reviewed the medical records of 82 girls with idiopathic CPP who had been treated with GnRHa at Severance Children's Hospital from 2004 to 2014.

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Purpose: The rapid increase in the incidence of precocious puberty in Korea has clinical and social significance. Gonadotropin-releasing hormone (GnRH) stimulation test is required to diagnose central precocious puberty (CPP), however this test is expensive and time-consuming. This study aimed to identify factors that can predict a positive response to the GnRH stimulation test.

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Purpose: Sex hormone-binding globulin (SHBG) modulates the availability of biologically active free sex hormones. The regulatory role of SHBG might be important in the relationship between hormone levels and the modification of lipid profiles in girls with precocious puberty. However, few studies have evaluated the relationship of SHBG, free estradiol index (FEI), and lipid levels in these girls.

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Purpose: It has been reported that daily recombinant human growth hormone (GH) treatment showed beneficial effects on growth in prepubertal children with idiopathic short stature (ISS). The present study aimed to validate the GH (Eutropin®) effect on growth promotion and safety after short-term GH treatment.

Materials And Methods: This study was an open-label, multicenter, interventional study conducted at nine university hospitals in Korea between 2008 and 2009.

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