Literature DB >> 19793313

Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.

Ingo Todt1, Juliette Mazereeuw-Hautier, Barbara Binder, Patrick J Willems.   

Abstract

The Keratitis-Ichthyosis-Deafness syndrome (KIDS) is an autosomal dominant ectodermal dysplasia characterized by ocular, skin, and ear anomalies, including keratitis, palmoplantar keratoderma, and congenital hearing loss. Most cases are due to mutations in the GJB2 gene encoding connexin 26. The Dandy-Walker malformation (DWM) is a developmental anomaly of the midline of the cerebellum with complete or partial agenesis of the vermis and cystic dilatation of the fourth ventricle. The association of KID syndrome with DWM has been reported a few times, but thought to be coincidental. We report 4 additional patients with KIDS and DWM, supporting the possibility that this is an association and not a coincidental finding. This also suggests that the GJB2 gene may have a role in other cases with DWM of, as yet, unknown etiology.

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Year:  2009        PMID: 19793313     DOI: 10.1111/j.1399-0004.2009.01211.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

1.  Structure and Functions of Gap Junctions and Their Constituent Connexins in the Mammalian CNS.

Authors:  E Yu Kirichenko; S N Skatchkov; A M Ermakov
Journal:  Biochem (Mosc) Suppl Ser A Membr Cell Biol       Date:  2021-06-10

2.  More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations.

Authors:  Evelyn Lilly; Christopher G Bunick; Alexander M Maley; Shali Zhang; Mary K Spraker; Amy J Theos; Karina L Vivar; Lucia Seminario-Vidal; Adam E Bennett; Robert Sidbury; Yasushi Ogawa; Masashi Akiyama; Barbara Binder; Smail Hadj-Rabia; Raffaella A Morotti; Earl J Glusac; Keith A Choate; Gabriele Richard; Leonard M Milstone
Journal:  J Am Acad Dermatol       Date:  2018-10-02       Impact factor: 11.527

Review 3.  Hearing loss in hydrocephalus: a review, with focus on mechanisms.

Authors:  David Satzer; Daniel J Guillaume
Journal:  Neurosurg Rev       Date:  2015-08-18       Impact factor: 3.042

4.  Mutant Cx30-A88V mice exhibit hydrocephaly and sex-dependent behavioral abnormalities, implicating a functional role for Cx30 in the brain.

Authors:  Nicole M Novielli-Kuntz; Eric R Press; Kevin Barr; Marco A M Prado; Dale W Laird
Journal:  Dis Model Mech       Date:  2021-01-26       Impact factor: 5.758

5.  Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome.

Authors:  Ambroise Wonkam; Jean Jacques N Noubiap; Jason Bosch; Collet Dandara; Geneviève Bengono Toure
Journal:  BMC Med Genet       Date:  2013-08-07       Impact factor: 2.103

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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