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Immunology

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation

Woojoong Kim, Eujin Park, Yo Han Ahn, Jiwon M. Lee, Hee Gyung Kang, Byung Joo Kim, Il-Soo Ha, Hae Il Cheong

Clin Exp Pediatr. 2016;59(Suppl 1):S5-S9. Published online November 30, 2016

Crossref 11

Blau syndrome (BS) is a rare autosomal dominant, inflammatory syndrome that is characterized by the clinical triad of granulomatous dermatitis, symmetric arthritis, and recurrent uveitis. Mutations in the nucleotide oligomerization domain 2 (NOD2) gene are responsible for causing BS. To date, up to 30 Blau-associated genetic mutations have been identified within this gene. We report a novel NOD2 genetic mutation...

DOI: https://doi.org/10.3345/kjp.2016.59.11.S5

Original Article

Intravenous fluid prescription practices among pediatric residents in Korea

Jiwon M. Lee, Younghwa Jung, Se Eun Lee, Jun Ho Lee, Kee Hyuck Kim, Ja Wook Koo, Young Seo Park, Hae Il Cheong, Il-Soo Ha, Yong Choi, Hee Gyung Kang

Clin Exp Pediatr. 2013;56(7):282-285. Published online July 19, 2013

Crossref 15

Purpose

Recent studies have established the association between hypotonic fluids administration and hospital-acquired hyponatremia in children. The present paper investigated the pattern of current practice in intravenous fluid prescription among Korean pediatric residents, to underscore the need for updated education.

Methods

A survey-based analysis was carried out. Pediatric residents at six university hospitals in Korea completed a survey consisting of four questions. Each...

DOI: https://doi.org/10.3345/kjp.2013.56.7.282

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