This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Review

. 1996;7(3):233-5.

Central nervous system abnormalities in oculodentodigital dysplasia

C T Schrander-Stumpel, C L Franke

PMID: 8897047

Review

Central nervous system abnormalities in oculodentodigital dysplasia

C T Schrander-Stumpel et al. Genet Couns. 1996.

. 1996;7(3):233-5.

Authors

C T Schrander-Stumpel, C L Franke

PMID: 8897047

No abstract available

PubMed Disclaimer

Similar articles

Clinical and genetic variability of oculodentodigital dysplasia.
Wiest T, Herrmann O, Stögbauer F, Grasshoff U, Enders H, Koch MJ, Grond-Ginsbach C, Schwaninger M. Wiest T, et al. Clin Genet. 2006 Jul;70(1):71-2. doi: 10.1111/j.1399-0004.2006.00631.x. Clin Genet. 2006. PMID: 16813608 No abstract available.
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
Amador C, Mathews AM, Del Carmen Montoya M, Laughridge ME, Everman DB, Holden KR. Amador C, et al. J Child Neurol. 2008 Aug;23(8):901-5. doi: 10.1177/0883073808317730. J Child Neurol. 2008. PMID: 18660473
Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly.
Richardson R, Donnai D, Meire F, Dixon MJ. Richardson R, et al. J Med Genet. 2004 Jan;41(1):60-7. doi: 10.1136/jmg.2003.012005. J Med Genet. 2004. PMID: 14729836 Free PMC article. No abstract available.
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature.
Taşdelen E, Durmaz CD, Karabulut HG. Taşdelen E, et al. Cytogenet Genome Res. 2018;154(4):181-186. doi: 10.1159/000489000. Epub 2018 Jun 15. Cytogenet Genome Res. 2018. PMID: 29902798 Review.
Oculodentodigital Dysplasia with a Novel Mutation in GJA1 Diagnosed by Targeted Gene Panel Sequencing: A Case Report and Literature Review.
Choi J, Yang A, Song A, Lim M, Kim J, Jang JH, Park KT, Cho S, Jin DK. Choi J, et al. Ann Clin Lab Sci. 2018 Nov;48(6):776-781. Ann Clin Lab Sci. 2018. PMID: 30610049 Review.

See all similar articles

Cited by

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement.
Harting I, Karch S, Moog U, Seitz A, Pouwels PJW, Wolf NI. Harting I, et al. AJNR Am J Neuroradiol. 2019 May;40(5):903-907. doi: 10.3174/ajnr.A6051. Epub 2019 May 2. AJNR Am J Neuroradiol. 2019. PMID: 31048294 Free PMC article.
Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47.
Abrams CK. Abrams CK. Biomolecules. 2023 Apr 21;13(4):712. doi: 10.3390/biom13040712. Biomolecules. 2023. PMID: 37189458 Free PMC article. Review.
Gap junctions in inherited human disease.
Zoidl G, Dermietzel R. Zoidl G, et al. Pflugers Arch. 2010 Jul;460(2):451-66. doi: 10.1007/s00424-010-0789-1. Epub 2010 Feb 7. Pflugers Arch. 2010. PMID: 20140684 Review.
Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.
Barzegar M, Sayadnasiri M, Tabrizi A. Barzegar M, et al. Iran J Child Neurol. 2012 Summer;6(3):39-43. Iran J Child Neurol. 2012. PMID: 24665271 Free PMC article.
Gap junctions in inherited human disorders of the central nervous system.
Abrams CK, Scherer SS. Abrams CK, et al. Biochim Biophys Acta. 2012 Aug;1818(8):2030-47. doi: 10.1016/j.bbamem.2011.08.015. Epub 2011 Aug 16. Biochim Biophys Acta. 2012. PMID: 21871435 Free PMC article. Review.

Publication types

Actions
Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Medical
- MedlinePlus Health Information