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A Case of C1 Inhibitor Deficiency Syndrome

Kim WH, Pahn YS, Kim NG, Oh KJ

  • KMID: 2275878
  • Korean J Otolaryngol-Head Neck Surg.
  • 2002 Feb;45(2):191-194.
C1 inhibitor (C1 INH) deficiency is characterized by recurrent attacks of angioedema. The disorder may be inherited or acquired, with both types presenting a similar phenotypic picture. The angioedema most...
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A Case of Dup (3q) Syndrome

Pahn YS, Choi MY, Lee YA, Chung WK, Lee KY, Oh SK

  • KMID: 2011662
  • J Korean Pediatr Soc.
  • 1997 Mar;40(3):408-412.
We have experienced a case of dup (3q) syndrome in the neonate who had a multiple congenital anomalies of hypertrichosis, hypertelorism, upslanting palpaberal fissures, anteverted nostrils, long philtrum, micrognathia, downturned...
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