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The Journal of Maternal-Fetal & Neonatal Medicine Volume 19, 2006 - Issue 7
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CaseReport

A rare cause of polyhydramnios: Neu–Laxova syndrome

Alicia Martín Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
,
Idoya Eguiluz Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
,
Miguel Á. Barber Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, SpainCorrespondence[email protected]
,
Norberto Medina Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
,
Walter Plasencia Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
,
Alfredo García-Alix Neonatology Unit, Paediatric Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
&
José A. García-Hernández Gynaecology and Obstetrics Department, University Hospital Materno Infantil of the Canaries, Las Palmas de Gran Canaria, Canary Islands, Spain
 show all
Pages 439-442 | Received 01 Jun 2005, Accepted 23 Nov 2005, Published online: 07 Jul 2009

References

  • Neu R, Kajii T, Gardner L, Nagyfy S, King S. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings. Pediatrics 1971; 47: 610–612
  • Laxova R, Ohara P, Timothy J. A further example of a lethal autosomal recessive condition in sibs. J Ment Defic Res 1972; 16: 139–143
  • Naveed M CS, Viyaja S. New manifestations of Neu–Laxova syndrome. Am J Med Genet 1999; 35: 55–57
  • Curry C J. Letter to the editor. Further comments on the Neu–Laxova syndrome. Am J Med Genet 1982; 13: 442–444
  • Fitch N, Resch L, Rochon L. The Neu–Laxova syndrome: Comments on syndrome identification. Am J Med Genet 1982; 13: 445–452
  • Mueller R F, Winter R M, Naylor C P. Letter to the editor. Neu–Laxova syndrome: Two further case reports and comments on proposed subclassification. Am J Med Genet 1983; 16: 645–649
  • Shapiro I, Borochowitz Z, Degani S, Dar H, Ibschitz I, Sharf M. Neu–Laxova syndrome: Prenatal ultrasonographic diagnosis, clinical and pathological studies, and new manifestations. Am J Med Genet 1992; 43: 602–605
  • Lazjuk G, Lurie I, Ostrowskaja T, Cherstvoy E, Kirillova I, Nedzved M, Usoev S. The Neu–Laxova syndrome: A distinct entity. Am J Med Genet 1979; 3: 261–267
  • Meguid N, Temtamy S. Neu Laxova syndrome in two Egyptian families. Am J Med Genet 1991; 41: 30–31
  • Gülmezoglu A, Ekici E. Sonographic diagnosis of Neu–Laxova syndrome. J Clin Ultrasound 1994; 22: 48–51

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