Dergiler / ENTcase / 2020 / Cilt: 6 - Sayı: 4

AN UNUSUAL CASE REPORT: UNEVENTFUL ADENOTONSILLECTOMY IN A WILLIAMS SYNDROME PATIENT WITH ADENOTONSILLAR HYPERTROPHY

WILLIAMS SENDROMLU ADENOTONSİLLER HİPERTROFİLİ HASTADA SORUNSUZ ADENOTONSİLLEKTOMİ

Dergi
ENTcase
Sayfa
126–130
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We present unproblematic adenotonsillectomy under general anesthesia in a child with WS and adenotonsillar hypertrophy.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Adenotonsillar disease is one of the most common diseases of childhood.
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Temel Bulgular & Veri:Williams-Beuren Syndrome (WS;OMIM 194050), also called Williams Syndrome is characterized by dysmorphic facial features, neurological findings and endocrinological abnormalities resulting from various lengths of deletions in the q11.23 region of the 7th chromosome.
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Sonuç & Katkı:We present unproblematic adenotonsillectomy under general anesthesia in a child with WS and adenotonsillar hypertrophy.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Adenotonsillar disease is one of the most common diseases of childhood. Children suffer from upper airway obstruction due to adenotonsillar hypertrophy as well as attacks of infection. Its clinical presentation ranges from mild recurrent infection to congestive heart failure. Williams-Beuren Syndrome (WS;OMIM 194050), also called Williams Syndrome is characterized by dysmorphic facial features, neurological findings and endocrinological abnormalities resulting from various lengths of deletions in the q11.23 region of the 7th chromosome. We present unproblematic adenotonsillectomy under general anesthesia in a child with WS and adenotonsillar hypertrophy.

Abstract

Adenotonsiller hastalık, çocukluk çağının en sık görülen hastalıklarından biridir. Çocuklar, adenotonsiller hipertrofiye bağlı üst solunum yolu tıkanıklığı ve enfeksiyon ataklarından müzdariptir. Klinik görünümü hafif tekrarlayan enfeksiyondan konjestif kalp yetmezliğine kadar değişir. Williams-Beuren Sendromu (WS;OMIM 194050) aynı zamanada Williams Syndrome olarak adlandırılan 7. kromozomun q11.23 bölgesindeki çeşitli uzunluktaki delesyonlardan kaynaklanan dismorfik yüz özellikleri, nörolojik bulgular ve endokrinolojik anormalliklerle karakterize bir sendromdur. Adenotonsiller hipertrofisi olan WS'li bir çocukta genel anestezi altında sorunsuz adenotonsillektomi sunuyoruz.

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Bu Makaleye Atıf Yap

BULUT, F., ŞİMŞEK, A. S., BALLICA, B. (2020). AN UNUSUAL CASE REPORT: UNEVENTFUL ADENOTONSILLECTOMY IN A WILLIAMS SYNDROME PATIENT WITH ADENOTONSILLAR HYPERTROPHY. ENTcase, Cilt: 6 - Sayı: 4, 126–130. https://ajindex.com/articles/150759

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Kaynakça (9)

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