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A Rare Case of Hyponatremia Caused by Reset Osmostat in a Neonate with Cleft Lip, Cleft Palate, and Imperforate Anus

  • Ahn, Jung Gu (Department of Pediatrics, Division of Pediatric Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Lee, Jeong Eun (Department of Pediatrics, Division of Pediatric Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Chung, Woo Yeong (Department of Pediatrics, Division of Pediatric Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Koo, Soo Hyun (Department of Pediatrics, Division of Pediatric Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Shin, Jaeho (Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Jeon, Ga Won (Department of Pediatrics, Division of Pediatric Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine)
  • 투고 : 2018.06.08
  • 심사 : 2018.08.13
  • 발행 : 2018.08.31

초록

Hyponatremia is defined as a plasma sodium concentration of <135 mEq/L. It is a common electrolyte imbalance in newborns. We report the case of a term neonate with cleft lip, cleft palate, imperforate anus, normal male karyotype, and chronic hyponatremia. On the 4th day of life, he showed hyponatremia (plasma sodium concentration 130 mEq/L) with low serum osmolality (275 mOsm/kg), high urine sodium (116.7 mEq/L), and high urine osmolality (412 mOsm/kg). His thyroid and adrenal functions were normal. Despite intravenous and oral sodium supplementation and hydrocortisone treatment, hyponatremia persisted. Brain magnetic resonance imaging showed normal results. He was diagnosed as having reset osmostat, a rare subtype of the syndrome of inappropriate secretion of antidiuretic hormone characterized by a subnormal threshold for antidiuretic hormone secretion, with hypotonic hyponatremia.

키워드

참고문헌

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