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There is a page named "CEDNIK syndrome" on Wikipedia

  • dysgenesis–neuropathy–ichthyosis–keratoderma syndrome is a neurocutaneous condition caused by mutation in the SNAP29 gene. CEDNIK syndrome is a rare congenital condition...
    6 KB (564 words) - 20:36, 20 April 2024
  • List of genetic syndromes
    )
    deficiency disorder". MedlinePlus. Retrieved 7 June 2021. "Orphanet: CEDNIK syndrome". Retrieved 8 May 2021. NIH Intramural Sequencing Center Group; Sloan...
    42 KB (969 words) - 16:02, 3 April 2024
  • They were characterized in 1975. CEDNIK syndrome (Cerebral Dysgenesis, Neuropathy, Ichthyosis and Keratoderma Syndrome) is a rare inherited genetic skin...
    3 KB (359 words) - 04:18, 23 April 2023
  • Thumbnail for Dolichol kinase deficiency
    gene. It is also known as Congenital disorder of glycosylation 1m. CEDNIK syndrome List of cutaneous conditions RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet:...
    2 KB (124 words) - 05:13, 5 May 2024
  • Thumbnail for Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
    retinoids is successful, but if treatment is stopped, symptoms recur. CEDNIK syndrome List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.;...
    4 KB (265 words) - 02:19, 7 May 2024
  • Thumbnail for SNAP29
    SNAP29 was shown to interact with CVB3 and EV-D68 viral protease 3C. CEDNIK Syndrome GRCh38: Ensembl release 89: ENSG00000099940 – Ensembl, May 2017 GRCm38:...
    9 KB (1,108 words) - 06:28, 18 December 2023