Publications by authors named "Duk-Hee Kim"

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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  • 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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  • The study explored the relationship between central obesity and sexual maturation in Korean girls with precocious puberty, analyzing data from 72 girls under 8 years old.
  • Increased visceral fat thickness (VFT) was linked to an earlier onset of breast development, but VFT levels were not significantly different between girls with central precocious puberty (CPP) and those without.
  • Overweight CPP girls displayed higher insulin resistance compared to their normal-weight peers, while insulin resistance levels did not vary in non-CPP girls based on weight.
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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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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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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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  • 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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  • 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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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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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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  • Turner syndrome (TS) is a chromosomal disorder that can lead to various cardiovascular issues, with vascular abnormalities being particularly common.
  • The case of a 9-year-old girl with TS, who experienced weakness in her legs due to spinal hemorrhage from a vascular malformation, highlights the rare occurrence of vertebral artery dissection in TS.
  • Immediate treatment with high-dose dexamethasone improved her ability to walk, emphasizing the importance of rapid diagnosis and MRI for suspected spinal vessel rupture in TS patients.
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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 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: In male patients with congenital adrenal hyperplasia (CAH), the presence of testicular adrenal rest tumors (TARTs) have been reported, however their prevalence and clinical manifestations are not well known. Untreated TARTs may lead to testicular structural damage and infertility. This study was conducted to investigate the prevalence of TARTs in male patients with CAH, and characterize the manifestations to identify contributing factors to TART.

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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: Short stature is a very common reason for visits to pediatric endocrine clinics. It could be the first sign of an underlying disease. The purpose of this study is to investigate the etiologies and general characteristics of subjects who visited an outpatient clinic due to short stature.

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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 (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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Longitudinal standards for height and height velocity are essential to monitor for appropriate linear growth. We aimed to construct standards in Korean children and adolescents through the population-based longitudinal Kangwha study. Our study was a part of a community-based prospective cohort study from 1986 to 1999 with 800 school children.

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