Familial Currarino syndrome associated with Hirschsprung disease: two cases of a mother and daughter.

[1]  J. Winberg,et al.  Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome. , 2011, Journal of pediatric surgery.

[2]  S. Borrego,et al.  Involvement of SOX10 in the pathogenesis of Hirschsprung disease: report of a truncating mutation in an isolated patient , 2010, Journal of Molecular Medicine.

[3]  S. Borrego,et al.  New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease , 2010, Genetics in Medicine.

[4]  S. Christian,et al.  Microcephaly, sensorineural deafness and Currarino triad with duplication–deletion of distal 7q , 2009, European Journal of Pediatrics.

[5]  Chih-ping Chen.  Syndromes, disorders and maternal risk factors associated with neural tube defects (IV). , 2008, Taiwanese journal of obstetrics & gynecology.

[6]  M. Pakarinen,et al.  Congenital funnel anus in children: associated anomalies, surgical management and outcome , 2007, Pediatric Surgery International.

[7]  J. Rozé,et al.  Currarino syndrome as an etiology of a neonatal Escherichia coli meningitis , 2007, Journal of Perinatology.

[8]  H. Urbach,et al.  Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia. , 2007, Birth defects research. Part A, Clinical and molecular teratology.

[9]  H. Nanjo,et al.  Split notochord syndrome: ileal duplication causing intermittent episodes of vomiting. , 2006, The Tohoku journal of experimental medicine.

[10]  O. Kilickesmez,et al.  Complete familial currarino triad in association with hirschsprung's disease: magnetic resonance imaging features and the spectrum of anorectal malformations , 2006, Acta radiologica.

[11]  C. Taecholarn,et al.  Currarino syndrome: report of two cases and review of the literature. , 2005, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

[12]  A. Capobianco,et al.  [The Currarino syndrome: two case reports]. , 2005, Minerva pediatrica.

[13]  V. Jasonni,et al.  Currarino syndrome: proposal of a diagnostic and therapeutic protocol. , 2004, Journal of pediatric surgery.

[14]  T. Ebisu,et al.  Neurenteric cysts with meningomyelocele or meningocele , 1990, Child's Nervous System.

[15]  G. Mavridis,et al.  Currarino triad associated with Hirschsprung's disease. , 2003, Journal of pediatric surgery.

[16]  L. Vanormelingen,et al.  In vitro high-field magnetic resonance imaging-documented anatomy of a fetal myelomeningocele at 20 weeks' gestation. A contribution to the rationale of intrauterine surgical repair of spina bifida. , 2003, Journal of neurosurgery.

[17]  A. Green,et al.  Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system. , 2003, Journal of pediatric surgery.

[18]  J. Osinga,et al.  A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction. , 1999, American journal of human genetics.

[19]  S. Scherer,et al.  A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis , 1998, Nature Genetics.

[20]  R. Azizkhan,et al.  A Novel Embryogenetic Mechanism for Currarino’s Triad: Inadequate Dorsoventral Separation of the Caudal Eminence from Hindgut Endoderm , 1998, Pediatric Neurosurgery.

[21]  P. Tam,et al.  Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease. , 1996, Human molecular genetics.

[22]  D. Pang,et al.  Sacral agenesis and caudal spinal cord malformations. , 1993, Neurosurgery.

[23]  W. Kirwan,et al.  Hereditary sacral agenesis with presacral mass and anorectal stenosis: The Currarino triad , 1991, The British journal of surgery.

[24]  S. Singh,et al.  Double split of notochord with massive prolapse of the gut. , 1988, Journal of pediatric surgery.

[25]  D. Coln,et al.  Triad of anorectal, sacral, and presacral anomalies. , 1981, AJR. American journal of roentgenology.

[26]  B. Duhamel.  From the Mermaid to Anal Imperforation: The Syndrome of Caudal Regression* , 1961, Archives of disease in childhood.