Literature DB >> 24209970

Multiple complex congenital malformations in a rabbit kit (Oryctolagus cuniculi).

Jennifer L Booth1, Xuwen Peng, Jennifer Baccon, Timothy K Cooper.   

Abstract

Congenital malformations may occur during early embryogenesis in cases of genetic abnormalities or various environmental factors. Affected subjects most often have only one or 2 abnormalities; subjects rarely have several unrelated congenital defects. Here we describe a case of a stillborn New Zealand white rabbit with multiple complex congenital malformations, including synophthalmia, holoprosencephaly, gastroschisis, and a supernumerary hindlimb, among other anomalies. There was no historical exposure to teratogens or other known environmental causes. Although not confirmed, this case was most likely a rare spontaneous genetic event.

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Year:  2013        PMID: 24209970      PMCID: PMC3750670     

Source DB:  PubMed          Journal:  Comp Med        ISSN: 1532-0820            Impact factor:   0.982


  26 in total

Review 1.  Supernumerary and absent limbs and digits of the lower limb: a review of the literature.

Authors:  Zachary Klaassen; Mohammadali M Shoja; R Shane Tubbs; Marios Loukas
Journal:  Clin Anat       Date:  2011-01-03       Impact factor: 2.414

2.  Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.

Authors:  E Roessler; E Belloni; K Gaudenz; P Jay; P Berta; S W Scherer; L C Tsui; M Muenke
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

3.  Teratogenic compounds of Veratrum californicum (Durand) X. Cyclopia in rabbits produced by cyclopamine.

Authors:  R F Keeler
Journal:  Teratology       Date:  1970-05

4.  Two cases of the caudal duplication anomaly including a discordant monozygotic twin.

Authors:  H Y Kroes; M Takahashi; R J Zijlstra; J A L L Baert; K A Kooi; R M W Hofstra; A J van Essen
Journal:  Am J Med Genet       Date:  2002-11-01

5.  Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.

Authors:  Gaurav G Mavinkurve; Daniel Sciubba; Eric Amundson; George I Jallo
Journal:  Childs Nerv Syst       Date:  2005-04-09       Impact factor: 1.475

Review 6.  Caudal duplication syndrome.

Authors:  R Dominguez; J Rott; M Castillo; R R Pittaluga; J N Corriere
Journal:  Am J Dis Child       Date:  1993-10

7.  Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.

Authors:  C Chiang; Y Litingtung; E Lee; K E Young; J L Corden; H Westphal; P A Beachy
Journal:  Nature       Date:  1996-10-03       Impact factor: 49.962

Review 8.  Chiari type I malformation: overview of diagnosis and treatment.

Authors:  John Nash; Joseph S Cheng; Glenn A Meyer; Bernd F Remler
Journal:  WMJ       Date:  2002

Review 9.  Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

Authors:  Mary Ella Pierpont; Craig T Basson; D Woodrow Benson; Bruce D Gelb; Therese M Giglia; Elizabeth Goldmuntz; Glenn McGee; Craig A Sable; Deepak Srivastava; Catherine L Webb
Journal:  Circulation       Date:  2007-05-22       Impact factor: 29.690

10.  Mechanisms of cardiac arrhythmias and sudden death in transgenic rabbits with long QT syndrome.

Authors:  Michael Brunner; Xuwen Peng; Gong Xin Liu; Xiao-Qin Ren; Ohad Ziv; Bum-Rak Choi; Rajesh Mathur; Mohammed Hajjiri; Katja E Odening; Eric Steinberg; Eduardo J Folco; Ekatherini Pringa; Jason Centracchio; Roland R Macharzina; Tammy Donahay; Lorraine Schofield; Naveed Rana; Malcolm Kirk; Gary F Mitchell; Athena Poppas; Manfred Zehender; Gideon Koren
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

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