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Results 1 - 10 of 22 for Vici syndrome
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  1. Vici syndrome 
    Vici syndrome is a severe disorder that begins early in life and affects many body systems. It is ... are less commonly affected.A characteristic feature of Vici syndrome is a brain abnormality called agenesis of the ...
    https://medlineplus.gov/genetics/condition/vici-syndrome - Genetics
  2. EPG5 gene 
    ... the EPG5 gene have been found to cause Vici syndrome, a severe condition that primarily affects the brain, ... the impairment leads to signs and symptoms of Vici syndrome. More About This Health Condition ectopic P granules ...
    https://medlineplus.gov/genetics/gene/epg5 - Genetics
  3. Skin Pigmentation Disorders (National Library of Medicine)  
    Pigmentation means coloring. Skin pigmentation disorders affect the color of your skin. Your skin gets its color from a pigment called melanin. Special cells in the ...
    https://medlineplus.gov/skinpigmentationdisorders.html - Health Topics
  4. Patient support and advocacy groups 
    ... VCFS Texas Vestibular Disorders Association VHL Family Alliance Vici Syndrome Organization Vitiligo Research Foundation Vitiligo Support International Wagner ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  5. Brain Malformations (National Library of Medicine)  
    Most brain malformations begin long before a baby is born. Something damages the developing nervous system or causes it to develop abnormally. Sometimes it's ...
    https://medlineplus.gov/brainmalformations.html - Health Topics
  6. Immune System and Disorders (National Library of Medicine)  
    What is the immune system? Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other ...
    https://medlineplus.gov/immunesystemanddisorders.html - Health Topics
  7. SLC25A15 gene 
    ... M, Boenzi S, Bertini E, Fiermonte G, Dionisi-Vici C. The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. Orphanet J Rare Dis. 2015 Mar 11;10: ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics
  8. Ornithine translocase deficiency 
    ... M, Boenzi S, Bertini E, Fiermonte G, Dionisi-Vici C. The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. Orphanet J Rare Dis. 2015 Mar 11;10: ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  9. ALDH18A1 gene 
    ... M, Fischer B, Ferrari P, Garavelli L, Dionisi-Vici C, Agolini E, Wischmeijer A, Morava E, Novelli G, Haberle J, Kornak U, Brancati F. De Barsy Syndrome: a genetically heterogeneous autosomal recessive cutis laxa syndrome ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
  10. DGUOK gene 
    ... DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome. Mol Genet Metab. 2009 Jul;97(3):221-6. doi: 10.1016/j.ymgme.2009.03.007. Epub 2009 Mar 27. Citation on PubMed Dimmock DP, Zhang Q, Dionisi-Vici C, Carrozzo R, Shieh J, Tang LY, Truong ...
    https://medlineplus.gov/genetics/gene/dguok - Genetics
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