- Review Articles
- Excessive crying: behavioral and emotional regulation disorder in infancy
- Joon Sik Kim
- Clin Exp Pediatr. 2011;54(6):229-233. Published online June 30, 2011
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In the pediatric literature, excessive crying has been reported solely in association with 3-month colic and is described, if at all, as unexplained crying and fussing during the first 3 months of life. The bouts of crying are generally thought to be triggered by abdominal colic (over-inflation of the still immature gastrointestinal tract), and treatment is prescribed accordingly. According to...
- Acute disseminated encephalomyelitis in children: differential diagnosis from multiple sclerosis on the basis of clinical course
- Yun Jin Lee
- Clin Exp Pediatr. 2011;54(6):234-240. Published online June 30, 2011
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Acute disseminated encephalomyelitis (ADEM) is a demyelinating disease of the central nervous system (CNS) that typically presents as a monophasic disorder associated with multifocal neurologic symptoms and encephalopathy. ADEM is considered an autoimmune disorder that is triggered by an environmental stimulus in genetically susceptible individuals. The diagnosis of ADEM is based on clinical and radiological features. Most children with ADEM...
- Mammalian target of rapamycin inhibitors for treatment in tuberous sclerosis
- Won Seop Kim
- Clin Exp Pediatr. 2011;54(6):241-245. Published online June 30, 2011
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Tuberous sclerosis complex (TSC) is a genetic multisystem disorder that results from mutations in the
TSC1 orTSC2 genes, and is associated with hamartomas in several organs, including subependymal giant cell tumors. The neurological manifestations of TSC are particularly challenging and include infantile spasms, intractable epilepsy, cognitive disabilities, and autism. TheTSC1 - andTSC2 -encoded proteins modulate cell function via the...
- Original Articles
- Outcomes of small for gestational age micropremies depending on how young or how small they are
- Hee Joon Yu, Eun Sun Kim, Jin Kyu Kim, Hye Soo Yoo, So Yoon Ahn, Yun Sil Chang, Won Soon Park
- Clin Exp Pediatr. 2011;54(6):246-252. Published online June 30, 2011
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Purpose The outcomes of small for gestational age (SGA) infants especially in extremely low birth weight infants (ELBWIs) are controversial. This study evaluated the mortality and morbidity of ELBWIs, focusing on whether or not they were also SGA.
Methods The medical records of 415 ELBWIs (birth weight <1,000 g), who were inborn and admitted to the Samsung Medical Center neonatal intensive care unit...
- The metabolic syndrome and body composition in childhood cancer survivors
- Young Bae Sohn, Su Jin Kim, Sung Won Park, Se-Hwa Kim, Sung-Yoon Cho, Soo Hyun Lee, Keon Hee Yoo, Ki Woong Sung, Jae Hoon Chung, Hong Hoe Koo, Dong-Kyu Jin
- Clin Exp Pediatr. 2011;54(6):253-259. Published online June 30, 2011
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Purpose Long-term survivors of childhood cancer appear to have an increased risk for the metabolic syndrome, subsequent type 2 diabetes and cardiovascular disease in adulthood compared to healthy children. The purpose of this study was to investigate the frequency of the metabolic syndrome and associated factors in childhood cancer survivors at a single center in Korea.
Methods We performed a retrospective review of...
- Clinical features of infantile hepatic hemangioendothelioma
- Eun Hee Kim, Kyung Nam Koh, Meerim Park, Bo Eun Kim, Ho Joon Im, Jong Jin Seo
- Clin Exp Pediatr. 2011;54(6):260-266. Published online June 30, 2011
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Purpose Infantile hepatic hemangioendothelioma (IHHE) is the most common type of hepatic vascular tumor in infancy. We conducted this study to review our clinical experience of patients with IHHE and to suggest management strategies.
Methods We retrospectively analyzed the medical records of 23 IHHE patients (10 males, 13 females) treated at the Asan Medical Center between 1996 and 2009.
Results Median age at diagnosis was...
- Case Reports
- A case of de novo duplication of 15q24-q26.3
- Eun Young Kim, Yu Kyong Kim, Mi Kyoung Kim, Ji Mi Jung, Ga Won Jeon, Hye Ran Kim, Jong Beom Sin
- Clin Exp Pediatr. 2011;54(6):267-271. Published online June 30, 2011
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Distal duplication, or trisomy 15q, is an extremely rare chromosomal disorder characterized by prenatal and postnatal overgrowth, mental retardation, and craniofacial malformations. Additional abnormalities typically include an unusually short neck, malformations of the fingers and toes, scoliosis and skeletal malformations, genital abnormalities, particularly in affected males, and, in some cases, cardiac defects. The range and severity of symptoms and physical...
- A sporadic case of Loeys-Dietz syndrome type I with two novel mutations of the
TGFBR2 gene - Jung Sook Ha, Yeo Hyang Kim
- Clin Exp Pediatr. 2011;54(6):272-275. Published online June 30, 2011
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A recently recognized connective tissue disorder, Loeys-Dietz syndrome (LDS) is a genetic aortic aneurysm syndrome caused by mutations in the transforming growth factor-receptor type I or II gene (
TGFBR1 orTGFBR2 ). They have distinctive phenotypic abnormalities including widely spaced eyes (hypertelorism), bifid uvula or cleft palate, and arterial tortuosity with aortic aneurysm or dissection throughout the arterial tree. LDS is...