Literature DB >> 11298377

Dandy-Walker variant in Coffin-Siris syndrome.

T Imai1, H Hattori, M Miyazaki, Y Higuchi, S Adachi, T Nakahata.   

Abstract

We describe a five-month-old male infant with Coffin-Siris syndrome, the so-called Dandy-Walker variant (hypoplasia of the cerebellar vermis with cystic dilatation of the fourth ventricle, but without enlargement of the posterior fossa), and partial agenesis of the corpus callosum. Dandy-Walker malformation and mega cisterna magna, but not Dandy-Walker variant, have been reported in Coffin-Siris syndrome. The presence of Dandy-Walker variant in the infant we described confirms that the full continuum of the Dandy-Walker complex can occur in Coffin-Siris syndrome. The yet unidentified gene(s) for the syndrome may be related to the development of the hindbrain. Copyright 2001 Wiley-Liss, Inc.

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Mesh:

Year:  2001        PMID: 11298377     DOI: 10.1002/ajmg.1231

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  The Coffin-Siris syndrome: a proposed diagnostic approach and assessment of 15 overlapping cases.

Authors:  Samantha A Schrier; Joann N Bodurtha; Barbara Burton; Albert E Chudley; Mary Anne D Chiong; Maria Gabriella D'avanzo; Sally Ann Lynch; Antonio Musio; Dmitriy M Nyazov; Pedro A Sanchez-Lara; Stavit A Shalev; Matthew A Deardorff
Journal:  Am J Med Genet A       Date:  2012-06-18       Impact factor: 2.802

2.  Camk2a-Cre-mediated conditional deletion of chromatin remodeler Brg1 causes perinatal hydrocephalus.

Authors:  Mou Cao; Jiang I Wu
Journal:  Neurosci Lett       Date:  2015-04-27       Impact factor: 3.046

Review 3.  The role of ARID1B, a BAF chromatin remodeling complex subunit, in neural development and behavior.

Authors:  Jeffrey J Moffat; Eui-Man Jung; Minhan Ka; Amanda L Smith; Byeong Tak Jeon; Gijs W E Santen; Woo-Yang Kim
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2018-08-24       Impact factor: 5.067

4.  Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment.

Authors:  Cemre Celen; Jen-Chieh Chuang; Xin Luo; Nadine Nijem; Angela K Walker; Fei Chen; Shuyuan Zhang; Andrew S Chung; Liem H Nguyen; Ibrahim Nassour; Albert Budhipramono; Xuxu Sun; Levinus A Bok; Meriel McEntagart; Evelien F Gevers; Shari G Birnbaum; Amelia J Eisch; Craig M Powell; Woo-Ping Ge; Gijs We Santen; Maria Chahrour; Hao Zhu
Journal:  Elife       Date:  2017-07-11       Impact factor: 8.140

5.  Neuroanatomy and behavior in mice with a haploinsufficiency of AT-rich interactive domain 1B (ARID1B) throughout development.

Authors:  J Ellegood; S P Petkova; J L Silverman; J P Lerch; A Kinman; L R Qiu; A Adhikari; A A Wade; D Fernandes; Z Lindenmaier; A Creighton; L M J Nutter; A S Nord
Journal:  Mol Autism       Date:  2021-03-23       Impact factor: 7.509

6.  Blake's pouch cyst and Werdnig-Hoffmann disease: Report of a new association and review of the literature.

Authors:  Sherien A Shohoud; Waleed A Azab; Tarek M Alsheikh; Rania M Hegazy
Journal:  Surg Neurol Int       Date:  2014-08-21
  6 in total

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