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Yenidoğan Döneminde Görülen Bir Uzun QT Sendromu Vakası

A case of Long QT Syndrome In A Neonate

Journal Name:

  • İnönü Üniversitesi Tıp Fakültesi Dergisi

Publication Year:

  • 2002

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Long QT syndrome is a rare cardiac defect characterised by syncope, life threatening tachyarrhytmias and sudden death. Although long QT syndrome has mostly been reported among adults, there are children presenting with this syndrome as well. We report a newborn baby presenting with long QT on electrocardiography and having polymorphic tachyarrhytmia causing death of the case.
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Abstract (Original Language): 
Uzun QT sendromu, hayatı tehdit eden taşiaritmiler ve ani ölüm ile karakterize olan, nadir görülen kardiak bir bozukluktur. Çocuklarda bildirilen uzun QT sendromu vakaları yetişkinlere oranla çok nadirdir. Burada yenidoğan servisinde prematüre doğum nedeniyle takip edilirken QT uzunluğu olan ve ventriküler aritmi ile kaybedilen bir hastayı sunacağız.
FULL TEXT (PDF): 
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  • 4
277-279
  • Turkish

REFERENCES

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