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Dergiler / The Journal of Pediatric Research / 2018 / Cilt: 5 - Sayı: 2

Sturge-Weber Syndrome Type III

Hande Gazeteci TEKİN
SARENUR GÖKBEN
SANEM KESKİN YILMAZ
Hasan TEKGÜL
Gül SERDAROĞLU
Sayfa
103–105
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We aim to present the case of an infant with SWS, which unlike the classical form was unidentifiable in physicalexamination and diagnosed using imaging methods

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live births.
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Temel Bulgular & Veri:A 5.5-month-old male patient with normalneuromotor development presented with right sided partial seizures, which had been occurring frequently for the previous two days and couldnot be controlled.
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Sonuç & Katkı:We aim to present the case of an infant with SWS, which unlike the classical form was unidentifiable in physicalexamination and diagnosed using imaging methods
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live births. The less common form, which canbe difficult to diagnose and only involves leptomeningeal angioma, has been defined as Type III SWS. A 5.5-month-old male patient with normalneuromotor development presented with right sided partial seizures, which had been occurring frequently for the previous two days and couldnot be controlled. A cranial magnetic resonance imaging showed pathological contrasts in the cortical regions involving the left hemisphere andin the leptomeningeal structures. We aim to present the case of an infant with SWS, which unlike the classical form was unidentifiable in physicalexamination and diagnosed using imaging methods

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Bu Makaleye Atıf Yap

TEKİN, H. G., GÖKBEN, S., YILMAZ, S. K., TEKGÜL, H., SERDAROĞLU, G. (2018). Sturge-Weber Syndrome Type III. The Journal of Pediatric Research, Cilt: 5 - Sayı: 2, 103–105. https://ajindex.com/articles/362803

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Kaynakça (9)

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