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Results 1 - 5 of 5 for SIDS
  1. TSPYL1 gene 
    ... Based on its role in a condition called sudden infant death with dysgenesis of the testes syndrome, researchers propose ... TSPYL1 gene has caused all identified cases of sudden infant death with dysgenesis of the testes syndrome (SIDDT), a ...
    https://medlineplus.gov/genetics/gene/tspyl1 - Genetics
  2. KCNQ1 gene 
    ... other conditions related to heart rhythm abnormalities, including sudden infant death syndrome (SIDS) and acquired long QT syndrome.SIDS is a major cause of death in babies ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  3. SCN5A gene 
    ... have also been identified in some cases of sudden infant death syndrome (SIDS). SIDS is a major cause of death in babies ... changes in the SCN5A gene could contribute to SIDS. Other genetic and environmental factors, many of which ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  4. MT-TL1 gene 
    ... identified in a small number of cases of sudden infant death syndrome (SIDS), which is a major cause of death in ... TL1 PubMed TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1 SUDDEN INFANT DEATH SYNDROME NCBI Gene ClinVar Betts J, Jaros E, ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  5. GJA1 gene 
    ... died suddenly with no known cause in infancy (sudden infant death syndrome) or early adulthood (sudden unexplained nocturnal death). ... Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death. Circulation. 2012 Jan 24;125(3):474-81. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics