Literature DB >> 30793783

CEDNIK syndrome in an Indian patient with a novel mutation of the SNAP29 gene.

Shital Poojary1, Kapisha S Shah1, Krishna B Bhalala1, Anaita Udwadia Hegde2.   

Abstract

CEDNIK (CErebral Dysgenesis, Neuropathy, Ichthyosis, and Keratoderma) syndrome is a neuroichthyotic syndrome characterized by a constellation of clinical features including severe developmental retardation, microcephaly, and facial dysmorphism. Here, we report the first case of CEDNIK syndrome from India presenting with characteristic clinical features and harboring a novel mutation of SNAP29 gene.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  SNAP29 gene; cerebral dysgenesis, neuropathy, ichthyosis, and keratoderma syndrome; ichthyosis; mental retardation

Mesh:

Substances:

Year:  2019        PMID: 30793783     DOI: 10.1111/pde.13761

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  3 in total

Review 1.  Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking.

Authors:  Matteo Gasparotto; Yi-Shin Lee; Alessandra Palazzi; Marcella Vacca; Francesco Filippini
Journal:  Biomolecules       Date:  2022-04-23

2.  New Cohort of Patients With CEDNIK Syndrome Expands the Phenotypic and Genotypic Spectra.

Authors:  Annelise Y Mah-Som; Cristina Skrypnyk; Andrea Guerin; Raafat Hammad Seroor Jadah; Vinayak Nivrutti Vardhan; Robert C McKinstry; Marwan S Shinawi
Journal:  Neurol Genet       Date:  2021-01-12

Review 3.  Sugary Logistics Gone Wrong: Membrane Trafficking and Congenital Disorders of Glycosylation.

Authors:  Peter T A Linders; Ella Peters; Martin Ter Beest; Dirk J Lefeber; Geert van den Bogaart
Journal:  Int J Mol Sci       Date:  2020-06-30       Impact factor: 5.923

  3 in total

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