Literature DB >> 8960322

Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome.

M Hayashi1, K Sakamoto, K Kurata, J Nagata, J Satoh, Y Morimatsu.   

Abstract

Little is known about the neuropathology of Cornelia de Lange syndrome. We report a unique type of cerebral malformation combined with Cornelia de Lange syndrome in a 5-year-old female child. At autopsy, the optic systems, hypothalamic nuclei, corpus callosum and cerebellar vermis were hypoplastic, and the septum pellucidum, fornix and anterior commissure were rudimentary. The brain had malformative features of septo-optic dysplasia combined with commissural dysplasia and cerebellar vermian hypoplasia. This case suggests an interrelationship between Cornelia de Lange syndrome and midline development of the brain.

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Mesh:

Year:  1996        PMID: 8960322     DOI: 10.1007/s004010050571

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  9 in total

Review 1.  Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature.

Authors:  Samantha A Schrier; Ilana Sherer; Matthew A Deardorff; Dinah Clark; Lynn Audette; Lynette Gillis; Antonie D Kline; Linda Ernst; Kathleen Loomes; Ian D Krantz; Laird G Jackson
Journal:  Am J Med Genet A       Date:  2011-11-08       Impact factor: 2.802

2.  Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.

Authors:  Tamanna R Roshan Lal; Mark A Kliewer; Thelma Lopes; Susan L Rebsamen; Julia O'Connor; Marco A Grados; Amy Kimball; Julia Clemens; Antonie D Kline
Journal:  Am J Med Genet C Semin Med Genet       Date:  2016-05-10       Impact factor: 3.908

3.  Neuroimaging features of Cornelia de Lange syndrome.

Authors:  Matthew T Whitehead; Usha D Nagaraj; Phillip L Pearl
Journal:  Pediatr Radiol       Date:  2015-02-21

4.  Focal congenital hyperinsulinism in a patient with septo-optic dysplasia.

Authors:  Raja Padidela; Ritika R Kapoor; Yuva Moyo; Clare Gilbert; Sarah E Flanagan; Sian Ellard; Khalid Hussain
Journal:  Nat Rev Endocrinol       Date:  2010-09-14       Impact factor: 43.330

Review 5.  Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome.

Authors:  Shimako Kawauchi; Rosaysela Santos; Akihiko Muto; Martha E Lopez-Burks; Thomas F Schilling; Arthur D Lander; Anne L Calof
Journal:  Am J Med Genet C Semin Med Genet       Date:  2016-04-27       Impact factor: 3.908

6.  Reliable callosal measurement: population normative data confirm sex-related differences.

Authors:  Tejal N Mitchell; Samantha L Free; Martin Merschhemke; Louis Lemieux; Sanjay M Sisodiya; Simon D Shorvon
Journal:  AJNR Am J Neuroradiol       Date:  2003-03       Impact factor: 3.825

7.  Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome.

Authors:  Shimako Kawauchi; Anne L Calof; Rosaysela Santos; Martha E Lopez-Burks; Clint M Young; Michelle P Hoang; Abigail Chua; Taotao Lao; Mark S Lechner; Jeremy A Daniel; Andre Nussenzweig; Leonard Kitzes; Kyoko Yokomori; Benedikt Hallgrimsson; Arthur D Lander
Journal:  PLoS Genet       Date:  2009-09-18       Impact factor: 5.917

8.  Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts.

Authors:  A Pistocchi; G Fazio; A Cereda; L Ferrari; L R Bettini; G Messina; F Cotelli; A Biondi; A Selicorni; V Massa
Journal:  Cell Death Dis       Date:  2013-10-17       Impact factor: 8.469

Review 9.  Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.

Authors:  Laura Avagliano; Paolo Grazioli; Milena Mariani; Gaetano P Bulfamante; Angelo Selicorni; Valentina Massa
Journal:  Orphanet J Rare Dis       Date:  2017-11-21       Impact factor: 4.123

  9 in total

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