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Gastrointestinal Anomalilerin Prenatal Tanisi
Serdar H. Ural, M.D., F.A.C.O.G. Director, Division of Maternal Fetal Medicine Director, Fellowship Training Program Medical Director, Labor and Delivery Unit Director, Obstetrical Ultrasound Unit Professor of Obstetrics & Gynecology and Radiology PennStateHealth University College of Medicine
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Anatomi/Fizyoloji 5-12. hafta embriyogenez Mide Yutkunma refleksi
Intestinal peristalsis Mekonyum Urogenital sinus Rektum
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Duodenal Atrezi
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Duodenal Atrezi -Duodenum tikanmasi -En sik konjenital ince bagirsak atrezisi -1/10,000 dogum, hafta embriyogenez -Diger anomaliler, kromozom, genetik -Down sendrom-%30 -Prognoz, cerrahi-diger hersey normalse iyi -Double bubble -Mide bosalmaz -Polihidramniyoz
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Duodenal Atresia+ polyhydramnios 31w GA: Maternal IDDM and T 21
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Doudenal Atresia
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#2
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#2 Same patient close to the end of the exam.
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Duodenal Atresia and Fetal Vomiting
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Ince Bagirsak Atrezisi, Mekonyum Ileus
Jejuno-ileal stenoz, volvulus Vaskuler Kistik fibroz-%25 Bagirsak dilatasyonu Polihidramniyoz
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Small Bowel Obstruction Bowel Atresia
The sites of small bowel atresia are: Proximal jejunum (31%) Distal jejunum (20%) Proximal ileum (13%) Distal ileum (36%) More than one site involved (6%).
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Dilated Fetal Bowel
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Gastrosizis -Paraumbilikal duvar defekti -1/4000 dogum
-Cogu zaman bagirsak sag taraf defektinden cikar -Kromozom riski az, ama sifir degil -Rupture omfalosel ihtimali -IUGG -Prognoz, cerrahi, iyi
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Gastroschisis
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Gastroschisis
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Gastroschisis
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Gastroschisis
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Dilated external bowel
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Omfalosel -Membran icinde bagirsak protruzyonu
-Abdominal duvar defekti-umbilikal kord cikis -1/4000 -Karaciger %80 -%60-70 diger anomaliler -%20-30 kromozom -Beckwith-Wiedemann sendromu; makrozomi -13. haftaya kadar fizyolojik herniyasyon -Prognoz
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Omphalocele
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Omphalocele
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Omphalocele
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Omphalcele
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Omphalocele
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Omphalocele
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Omphalocele
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Omphalocele
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Echogenic Bowel
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Echogenic Bowel
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Echogenic Bowel
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Echogenic Bowel
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Mekonyum Peritonit/Kist
Steril kimyasal/enflamasyon sonucu bagirsak perforasyonu Obstruksyona bagli Mekonyumun cikisi iritasyon sonucu kiste (kompleks gorunum olabilir) yol acar Kistik fibroz Vaskuler Polihidramniyoz bulunur Cogu zaman kendiliginden gecer, bazen cerrahi
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US at 27w MR at 28w Complex cyst with fluid- fluid level
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Enterik Duplikasyon Kisti
Herhangi bagirsak bolgesi Tubuler 1’den fazla Postnatal US: duodenal duplication cyst
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Mezenterik/Omental Kist
Abdominal lenfatik malformasyon Buyuk multilokuler kistik yapi Kompleks gorunum Vaskuler goruntu
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Mesenteric Cyst LUQ (Vascular Malformation, Lymphatic Type)
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Anal/Kolon/Kloakal Atrezi
Iskemi 1/500 Genetik VACTERL birlesimi; vertebral defekt, anal atrezi, trakeoozofagal fistul, renal displazi Alkol, diyabet Prognoz %90
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Persistent Cloaca US Prenatal Diagnosis
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Colonic Atresia Dilated bowel (1st detected at 23w US). Echogenic content and haustral pattern to level of expected distal transverse colon. AFI was normal (18.7cm at 30w)
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Colonic Atresia
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Intraluminal Kalsifikasyon
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Case #6
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Case #6 Bladder Normal mesane mevcut
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-Ultrason oldukca faydali -Tani deneyimli ellerde emin
GI Anomaliler -Ultrason oldukca faydali -Tani deneyimli ellerde emin -Tarama/invaziv yontemler kesin teshis -Ultrason takibi cok onemli; komplikasyon taramasi (polihidramniyoz); dogum zamanlamasi -Hasta danismanligi
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