Abstract
Three members of a family in two generations with proximal jejunal atresia and renal dysplasia are described. This association is presumably an autosomal dominant condition.
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Blake NS, Puri P (1986) Hereditary multiple atresias: radiological and pathological aspects. Ann Radiol 8: 656
deLorimer AA, Fonkalsrud EW, Hays DM (1969) Congenital atresia and stenosis of the jejunum and ileum. Surgery 65: 819
Louw JH, Barnard CN (1955) Congenital intestinal atresia, observations and its origin. Lancet 2: 1065–1067
Rescorla FJ, Grosfeld JL (1985) Intestinal atresia and stenosis: analysis of survival in 120 cases. Surgery 98: 698
Weiss RG, Ryan DP, Ilstad ST, Noseworth J, Martin LW (1990) A complex case of jejunoileocolic atresias. J Pediatr Surg 25: 560
Guttman FM, Braun P, Garance PH, Blanchard H, Collin PP, Dallaire L, Desjardins JG, Perreault G (1973) Multiple atresias and a new syndrome of hereditary multiple atresias involving the gastrointestinal tract from stomach to rectum. J Pediatr Surg 8: 633
Rittenhouse EA, Beckwith JB, Chappell JS, Bill AH (1972) Multiple septa of the small bowel: description of an unusual case, with review of the literature and consideration of etiology. Surgery 71: 371
Schiavetti E, Massotti G, Torricelli M, Perfetti L (1984) “Apple peel” syndrome. A radiological study. Pediatr Radiol 14: 380
Seashore JH, Collins FS, Markowitz RI, Seashore MR (1987) Familial apple peel jejunal atresia: surgical, genetic and radiographic aspects. Pediatrics 80: 540
Rickham PP, Karplus M (1971) Familial and hereditary intestinal atresia. Helv Pediatr Acta 26: 561
Blyth H, Dickson JAS (1969) Apple peel syndrome (congenital intestinal atresia). A family study of seven index patients. J Med Genet 6: 275
Daneman A, Martin DJ (1979) A syndrome of multiple gastrointestinal atresias with intraluminal calcification. Pediatr Radiol 8: 227
Martin CE, Leonidas JC, Armoury RA (1976) Multiple gastro-intestinal atresias with intraluminal calcification and cystic dilatation of the bile ducts: a newly recognized entity resembling a string of pearls. Pediatrics 57: 268
McHugh K, Daneman A (1991) Multiple gastrointestinal atresias: sonography of associated biliary abnormalities. Pediatr Radiol 21: 355
Kao KJ, Flesicher R, Bradford WD, Woodward BH (1983) Multiple congenital septal atresias of the intestine: histomorphologic and pathogenetic implications. Pediatr Pathol 1: 443
Puri P, Guiney EJ, Carroll R (1985) Multiple gastrointestinal atresias in three consecutive siblings: observations on pathogenesis. J Pediatr Surg 20: 22
Teja K, Schnatterly P, Shaw A (1981) Multiple intestinal atresias: pathology and pathogenesis. J Pediatr Surg 16: 194
Bury F, Wilekens H, deWale P, Marchal G, Kerremans R, Eggermont E (1977) Aglossie-adactylie avec atrésie jéjunale. Arch Fr Pediatr 34: 604
David A, Rozé JC, Rédmond S, Branger B, Héloury Y (1992) Hypoglossia-Hypodactylia syndrome with jejunal tresia in an infant of a diabetic mother. Am J Med Genet 43: 882
Moorman-Voestermans CGM, Heij HA, Vos A (1990) Jejunal atresia in twins. J Pediatr Surg 25: 638
van der Pol JB, Wolf H, Boer K, Treffers PE, Leschot NJ, Hey HA, Vos A (1992) Jejunal atresia related to the use of methylene blue in genetic amniocentesis in twins. Br J Obstet Gynaecol 99: 141
Kissane JM (1990) Renal cysts in pediatric patients: a classification and overview. Pediatr Nephrol 4: 69
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Herman, T.E., Mc Alister, W.H. Familial type 1 jejunal atresias and renal dysplasia. Pediatr Radiol 25, 272–274 (1995). https://doi.org/10.1007/BF02011098
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DOI: https://doi.org/10.1007/BF02011098