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Results 1 - 10 of 72 for babies
  1. TSPYL1 gene 
    ... on its role in a condition called sudden infant death with dysgenesis of the testes syndrome, researchers ... gene has caused all identified cases of sudden infant death with dysgenesis of the testes syndrome (SIDDT), ...
    https://medlineplus.gov/genetics/gene/tspyl1 - Genetics
  2. UGT1A1 gene 
    ... usually disappear in 1 to 2 weeks. Some babies develop kernicterus (which can be lethal), hearing loss, ... with breastfeeding: Unconjugated bilirubin levels increase when the baby is breastfed, causing jaundice, and return to normal ...
    https://medlineplus.gov/genetics/gene/ugt1a1 - Genetics
  3. KCNQ1 gene 
    ... 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 younger than one year. It is characterized by ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  4. ALOX12B gene 
    ... another form of ichthyosis called self-healing collodion baby. Individuals with this condition are born with a ... during the first few weeks of life. While babies with NBCIE (described above) may also be born ...
    https://medlineplus.gov/genetics/gene/alox12b - Genetics
  5. NDP gene 
    ... eye disorder that leads to blindness in male infants at birth or soon after birth. The NDP ... of a retinal disorder that affects some premature infants. Retinopathy of prematurity is a condition in which ...
    https://medlineplus.gov/genetics/gene/ndp - Genetics
  6. SCN5A gene 
    ... also been identified in some cases of sudden infant death syndrome (SIDS). SIDS is a major cause of death in babies younger than 1 year. It is characterized by ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  7. CYB5R3 gene 
    ... has been associated with low methemoglobin levels in infants who were born prematurely and treated with nitric ... prevent chronic lung disease. The lungs of premature infants are often underdeveloped and need support after birth. ...
    https://medlineplus.gov/genetics/gene/cyb5r3 - Genetics
  8. CASR gene 
    ... a potentially fatal condition that becomes apparent in infants under the age of 6 months. Affected babies often have overgrowth of one or more of ... gene variants in children: a case study of infant hypocalcaemia and literature review. Acta Paediatr. 2014 Nov; ...
    https://medlineplus.gov/genetics/gene/casr - Genetics
  9. LCT gene 
    ... In this disorder (also known as congenital alactasia), infants are unable to break down lactose in breast milk or formula. Infants who are unable to process lactose are considered ...
    https://medlineplus.gov/genetics/gene/lct - Genetics
  10. MT-TL1 gene 
    ... in a small number of cases of sudden infant death syndrome (SIDS), which is a major cause ... PubMed TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1 SUDDEN INFANT DEATH SYNDROME NCBI Gene ClinVar Betts J, Jaros ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
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