Visceral malformations

Articles

• neurenteric cyst
  10 February 2006

  Definition: A neurenteric cyst is a rare congenital disorder secondary to alimentary duplication and vertebral malformation.
  Neurenteric cysts are extremely rare congenital anomalies, often presenting in the first 5 years of life, and
  Neurenteric cysts are caused by an incomplete separation of the notochord from the foregut during the third week of embryogenesis.
  Neurenteric cyst are frequently accompanied with spinal or gastrointestinal abnormalities, but the latter may be absent in (...)

• intestinal atresia
  9 February 2005

  jejunoileal atresia (JIA)

• splenotesticular fusion
  16 March 2011

  Digital slides
  Case 19 : Spleno-testicular fusion
  Synopsis
  splenogonadal fusion
  elongated spleen connected with gonad (testsi or ovary) possible colonic compression or stricture
  splenic nodule on gonad
  continuous splenic tissue from left hypochondre to gonad
  Associations
  limb deficiency (#9386063#) ectromelia
  micrognathia (#9386063#)
  See also
  splenic malformations
  References
  Splenogonadal fusion with limb deficiency and micrognathia. Moore PJ, Hawkins EP, Galliani (...)

• horseshoe kidney
  21 May 2004

  Associations (Examples)
  chromosomal anomalies monosomy X (Turner syndrome)
  neurofibromatosis type 1 (von Recklinhausen disease) NF1-associated horseshoe kidney (#15150783#, #417177#)
  malformations anorectal malformations anorectal agenesis with annal imperforation
  tumors rhabdomyosarcoma (#3277029#)
  Case records
  Case 10298
  See also
  solitary kidney (unique kidney)
  renal (...)

• ureteral duplication
  21 May 2004

  Features
  ureteral malformations

• renal hypodysplasia
  9 February 2007

  Definition: Renal hypodysplasia (RHD) is characterized by reduced kidney size and maldevelopment of the renal tissue following abnormal organogenesis.
  Renal hypodyspasia associates bilateral non-obstructive renal dysplasia (BNORD) and bilateral non-obstructive renal hypoplasia(BNORH).
  Renal hypodysplasia is characterized by a decrease in nephron number, a small overall kidney size, and a maldeveloped renal tissue.
  Types
  non-syndromal renal hypodysplasia (HP.10934) (MIM.610805) (...)

• unilateral renal ectopia
  28 January 2008

  Definition: renal ectopia limited to one side.
  See also
  renal ectopia
  renal malformations
  anomalies of renal position

• megacalyces
  21 March 2007

  Types
  familial megacalyces
  Associations
  Hirschsprung disease (#1246788#)
  References
  Lam AH. Familial megacalyces with autosomal recessive inheritance. Report of 3 affected siblings. Pediatr Radiol. 1988;19(1):28-30. PMID: #3222059#

• ovotesticular DSD
  19 October 2007

  ovotesticular disorder of sexual differentiation, true hermaphroditism, true hermaphrodism

• supernumerary pulmonary lobe
  15 December 2005

  pulmonary lobes

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