Zobrazeno 1 - 10
of 36
pro vyhledávání: '"59"'
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 12, Pp 483-489 (2016)
Korean Journal of Pediatrics
Korean Journal of Pediatrics
Purpose We investigated the number of test takers of the Korean-Developmental Screening Test (K-DST) in a single children's hospital within a year, according to age, referral rate, and follow-up percentage. Methods For this study, 4,062 children who
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S80-S83 (2016)
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S80-S83 (2016)
Isolated anomalous right coronary artery originating from the pulmonary artery (ARCAPA) is a rare congenital coronary anomaly that is asymptomatic and discovered incidentally in most cases. ARCAPA is generally not considered a fatal defect in infancy
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S64-S67 (2016)
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S64-S67 (2016)
Congenital tuberculosis (TB) is a rare disease that is associated with high mortality. Mycobacterium tuberculosis, the causative agent, may be transmitted from the infected mother to the fetus by the transplacental route or by aspiration of infected
Prognostic factors of neurological outcomes in late-preterm and term infants with perinatal asphyxia
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 11, Pp 440-445 (2016)
Korean Journal of Pediatrics
Korean Journal of Pediatrics
PURPOSE This study aimed to identify prognostic factors of neurological outcomes, including developmental delay, cerebral palsy and epilepsy in late-preterm and term infants with perinatal asphyxia. METHODS All late-preterm and term infants with peri
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss 11, Pp 456-459 (2016)
Korean Journal of Pediatrics, Vol 59, Iss 11, Pp 456-459 (2016)
Triple-A syndrome, also known as Allgrove syndrome, is a rare autosomal recessive disorder. The 3 features of this syndrome are achalasia, adrenal insufficiency, and alacrima. Achalasia could be the first manifestation of the triple-A syndrome; howev
Autor:
Jae Woo Lim, Kyung Ok Ko, Jung Min Yoon, Young Jin Kim, Eun Jeong Cheon, Jang Sin Son, Ji Sun Lee
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S88-S91 (2016)
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S88-S91 (2016)
Esophageal granular cell tumor (GCT) is a rare neoplasm originating from the Schwann cells of the submucosal neuronal plexus. Histology is the gold standard for its diagnosis. Endoscopic resection or surgical excision should be considered, depending
Autor:
Ki Hwan Kim, Yu Mi Seo, Seung Beom Han, Myungshin Kim, Jin Han Kang, Nack Gyun Chung, Dae Chul Jeong, Jung Woo Rhim, Joon Hyeong Park
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss 10, Pp 421-424 (2016)
Korean Journal of Pediatrics, Vol 59, Iss 10, Pp 421-424 (2016)
Recurrent macrophage activation syndrome (MAS) is very rare. We present the case of an adolescent boy with human leukocyte antigen (HLA) B27-positive ankylosing spondylitis (AS), who experienced episodes of recurrent MAS since he was a toddler. A 16-
Autor:
Moo Sook Lee, Kyung Sue Shin
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 4, Pp 196-201 (2016)
Korean Journal of Pediatrics
Korean Journal of Pediatrics
Chronic granulomatous disease (CGD) is a rare inherited disorder caused by defective nicotinamide adenine dinucleotide phosphate oxidase enzyme and characterized by recurrent bacterial and fungal infections. Although liver abscess is a common manifes
Autor:
Byung Kyu Suh, Won Kyoung Cho
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 59, Iss 1, Pp 1-7 (2016)
Korean Journal of Pediatrics, Vol 59, Iss 1, Pp 1-7 (2016)
Infants born small for gestational age (SGA) are at increased risk of perinatal morbidity, persistent short stature, and metabolic alterations in later life. Recent studies have focused on the association between birth weight (BW) and later body comp
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
Autor:
Ja Hye Kim, Ja Hyang Cho, Jin-Ho Choi, Eul Ju Seo, Beom Hee Lee, Go Hun Seo, Han Wook Yoo, Gu-Hwan Kim
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 1, Pp 16-23 (2016)
Korean Journal of Pediatrics
Korean Journal of Pediatrics
Purpose: The 1p36 deletion syndrome is a microdeletion syndrome characterized by developmental delays/intellectual disability, craniofacial dysmorphism, and other congenital anomalies. To date, many cases of this syndrome have been reported worldwide