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Results 1 - 10 of 55 for compartment syndrome OR edema OR edema
  1. Bowen-Conradi syndrome 
    ... new proteins. Ribosomes are assembled in a cell compartment called the nucleolus.The particular EMG1 gene mutation known to cause Bowen-Conradi syndrome is thought to make the protein unstable, resulting ...
    https://medlineplus.gov/genetics/condition/bowen-conradi-syndrome - Genetics
  2. SLC9A6 gene 
    ... is important for the recycling function of these compartments. The NHE6 protein may have ... to Christianson syndrome. This condition is characterized by neurological problems, including ...
    https://medlineplus.gov/genetics/gene/slc9a6 - Genetics
  3. Action myoclonus–renal failure syndrome 
    ... compartments that digest and recycle materials. In these compartments, ... associated with AMRF syndrome lead to production of an altered LIMP-2 ...
    https://medlineplus.gov/.../action-myoclonus-renal-failure-syndrome - Genetics
  4. Hermansky-Pudlak syndrome 
    ... related organelles (LROs). LROs are very similar to compartments within the ... with Hermansky-Pudlak syndrome prevent the formation of LROs or impair the ...
    https://medlineplus.gov/genetics/condition/hermansky-pudlak-syndrome - Genetics
  5. TBC1D20 gene 
    ... important for maintaining the structure of a cell compartment called the Golgi apparatus, in ... been found to cause Warburg micro syndrome, which is the most severe of the disorders ...
    https://medlineplus.gov/genetics/gene/tbc1d20 - Genetics
  6. Christianson syndrome 
    ... people in other parts of the world. ... endosomes, which are compartments within cells that recycle proteins and other materials. ...
    https://medlineplus.gov/genetics/condition/christianson-syndrome - Genetics
  7. EMG1 gene 
    The EMG1 gene provides instructions for making a protein that is involved in the production of cellular structures called ribosomes, which process the cell' ...
    https://medlineplus.gov/genetics/gene/emg1 - Genetics
  8. SCARB2 gene 
    The SCARB2 gene provides instructions for making a protein called lysosomal integral membrane protein-2 (LIMP-2). As its name suggests, this protein is primarily ...
    https://medlineplus.gov/genetics/gene/scarb2 - Genetics
  9. Microcephaly-capillary malformation syndrome 
    ... been diagnosed with the disorder. ... surface to specialized cell compartments that break down (degrade) or recycle them. This ...
    https://medlineplus.gov/...rocephaly-capillary-malformation-syndrome - Genetics
  10. Hereditary folate malabsorption 
    ... proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and ... into systemic compartments and tissues. Expert Rev Mol Med. 2009 Jan ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
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