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Results 1 - 10 of 19 for SUDDEN INFANT DEATH SYNDROME
  1. Sudden infant death with dysgenesis of the testes syndrome 
    Sudden infant death with dysgenesis of the testes syndrome (SIDDT) is a rare condition that is fatal in the first year of life; its major features include abnormalities ...
    https://medlineplus.gov/...th-with-dysgenesis-of-the-testes-syndrome - Genetics
  2. 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
  3. KCNQ1 gene 
    ... other conditions related to heart rhythm abnormalities, including sudden infant death syndrome (SIDS) and acquired long QT syndrome.SIDS ... like subfamily, member 1 Tests of KCNQ1 PubMed SUDDEN INFANT DEATH SYNDROME POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  4. SCN5A gene 
    ... have also been identified in some cases of sudden infant death syndrome (SIDS). SIDS is a major cause of ... ALPHA SUBUNIT 5; SCN5A CARDIOMYOPATHY, DILATED, 1E; CMD1E SUDDEN INFANT DEATH SYNDROME VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1 ATRIAL ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  5. MT-TL1 gene 
    ... identified in a small number of cases of sudden infant death syndrome (SIDS), which is a major cause of ... 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
  6. 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
  7. TH gene 
    ... One TH gene polymorphism has been associated with sudden infant death syndrome (SIDS). SIDS is a major cause of ... gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. J Pediatr. 2008 Aug;153(2):190- ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  8. Congenital central hypoventilation syndrome 
    ... been identified. Researchers believe that some cases of sudden infant death syndrome (SIDS) or sudden unexplained death in children may be caused by ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
  9. Brugada syndrome 
    ... 40. This condition may explain some cases of sudden infant death syndrome (SIDS), which is a major cause of death in babies younger than 1 year. SIDS is characterized by sudden and unexplained death, usually during sleep.Sudden unexplained ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  10. Short QT syndrome 
    ... age. This condition may explain some cases of sudden infant death syndrome (SIDS), which is a major cause of unexplained death in babies younger than 1 year. However, some people with short QT syndrome ... QT syndrome or related heart problems and sudden cardiac death. Other cases of short QT syndrome ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
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