Journals / İstanbul Kanuni Sultan Süleyman Tıp Dergisi / 2016 / Cilt: 8 - Sayı: 2

Anaesthetic Management of a Child with Hallermann-Streiff-François Syndrome in the Operating Room and in a Remote Location

Hallermann-Streiff-François Sendromlu Çocukta Ameliyat Odası ve Ameliyat Odası Dışı Anestezi Yönetimi

Pages
117–120
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this article, we reported our anaesthetic management of a 4 -year- old patient with HSF syndrome who received general anesthesia for a total of 6 times due to congenital bilateral cataracts in operating room and in remote location.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hallermann-Streiff-François (HSF) syndrome is a genetic disorder with autosomal recessive inheritance which can cause dyscephaly, hypoplastic mandible, depressed nasal bridge, congenital cataracts and macroglossia.
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Key Findings & Data:These craniofacial anomalies may lead to upper airway obstruction and difficult airway.
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Conclusion & Impact:In this article, we reported our anaesthetic management of a 4 -year- old patient with HSF syndrome who received general anesthesia for a total of 6 times due to congenital bilateral cataracts in operating room and in remote location.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hallermann-Streiff-François (HSF) syndrome is a genetic disorder with autosomal recessive inheritance which can cause dyscephaly, hypoplastic mandible, depressed nasal bridge, congenital cataracts and macroglossia. These craniofacial anomalies may lead to upper airway obstruction and difficult airway. In this article, we reported our anaesthetic management of a 4 -year- old patient with HSF syndrome who received general anesthesia for a total of 6 times due to congenital bilateral cataracts in operating room and in remote location.

Özet

Hallermann-Streiff-François (HSF) sendromu sporadik olarak ortaya çıkan mikrosefali, seyrek saç ve kaş, mikroftalmi, katarakt, ince cilt, ince ve sivri burun ve mikrognati gibi kraniofasiyal bulguların yanısıra trakeomalazi, sık pulmoner infeksiyon ve ince ve osteopenik kemik yapısı ile karakterize bir genetik bozukluktur. Bu anomaliler üst hava yolu obstrüksiyonu ve zor entübasyona neden olabilmektedir. Bu makalede konjenital bilateral katarakt nedeniyle toplam 6 kez genel anestezi almış 4 yaşındaki HSF sendromlu bir hastada ameliyat odası ve ameliyat odası dışındaki anestezi yönetimimiz anlatılmaktadır.

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Cite This Article

TÜYSÜZ, B., BEYOĞLU, Ç. A., GÜNGÖR, G., TUNALI, Y., BOZKURT, P. S., BEYOĞLU, İ. (2022). Anaesthetic Management of a Child with Hallermann-Streiff-François Syndrome in the Operating Room and in a Remote Location. İstanbul Kanuni Sultan Süleyman Tıp Dergisi, Cilt: 8 - Sayı: 2, 117–120. https://ajindex.com/articles/551134

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References (6)

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