✦ LIBER ✦

Aganglionosis of the entire bowel: Four new cases and review of the literature

✍ Scribed by Maria Di Lorenzo; S. Yazbeck; P. Brochu

Publisher: John Wiley and Sons
Year: 1985
Tongue: English
Weight: 224 KB
Volume: 72
Category: Article
ISSN: 0007-1323
DOI: 10.1002/bjs.1800720825

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract
Four cases of aganglionosis of the entire bowel are presented, each with their histological characteristics, all invariably lethal.

📜 SIMILAR VOLUMES

Fetal acrania: Five new cases and review

Fetal acrania: Five new cases and review of the literature

✍ Weissman, Amir; Diukman, Rony; Auslender, Ron 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 2 views

Acrania is a lethal malformation in which there is an absence of the flat skull bones covering the brain. Five new cases are described, and a review of the English-language medical literature is presented. The sonographic differential diagnosis of acrania includes anencephaly, large cephalocele, ost

Calcification of the fetal heart—four ca

Calcification of the fetal heart—four case reports and a literature review

✍ Julia Hajdu; Tamas Marton; Csaba Papp; Ervin Hruby; Zoltan Papp 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 229 KB 👁 2 views

Calcification of the heart and vessels in fetuses is a rare condition. It may be dystrophic or metastatic. An extremely rare form of vascular calcification has been termed 'idiopathic arterial calcification of infancy', which is inherited in an autosomal recessive pattern. We report four cases of my

Three new cases of the Schinzel-Giedion

Three new cases of the Schinzel-Giedion syndrome and review of the literature

✍ Labrune, Philippe ;Lyonnet, Stanislas ;Zupan, Véronique ;Imbert, Marie-Claire ;G 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 419 KB 👁 2 views

Hemoglobin S/OARAB: Thirteen new cases a

Hemoglobin S/OARAB: Thirteen new cases and review of the literature

✍ Zimmerman, Sherri A.; O'Branski, Erin E.; Rosse, Wendell F.; Ware, Russell E. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 354 KB 👁 2 views

Hemoglobin S/O Arab (Hb S/O Arab ) is a rare compound heterozygous hemoglobinopathy characterized by the presence of two variant ␤-globin chains: ␤ 6 Glu → Val (Hb S) and ␤ 121 Glu → Lys (Hb O Arab ). The diagnosis of Hb S/O Arab requires electrophoresis on both cellulose acetate and citrate agar, s

Setleis syndrome: Three new cases and a

Setleis syndrome: Three new cases and a review of the literature

✍ McGaughran, Julie ;Aftimos, Salim 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 275 KB 👁 2 views

New cases of Bohring–Opitz syndrome, upd

New cases of Bohring–Opitz syndrome, update, and critical review of the literature

✍ Axel Bohring; Grétel G. Oudesluijs; Dorothy K. Grange; Giuseppe Zampino; Patrick 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 231 KB 👁 2 views