Prenatally closed gastroschisis with midgut atresia
Pediatric Surgery International, cilt.18, sa.5-6, ss.550-552, 2002 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 18 Sayı: 5-6
- Basım Tarihi: 2002
- Doi Numarası: 10.1007/s00383-002-0815-2
- Dergi Adı: Pediatric Surgery International
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.550-552
- Anahtar Kelimeler: Fetal abdominal-wall closure, Gastroschisis, Intestinal atresia, Short-bowel syndrome
- Trakya Üniversitesi Adresli: Evet
Özet
Spontaneous prenatal closure of gastroschisis (GS) is rare and usually associated with atresia of the midgut. We describe a case of GS diagnosed at 20 weeks' gestation that resolved spontaneously in utero. At delivery the infant had an ileus. A laparotomy with a jejunocolostomy was performed, but she died at 2 months of age due to complications of total parenteral nutrition. © Springer-Verlag 2002.