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Results 1 - 10 of 69 for Premature birth
  1. Bartter syndrome 
    ... fetus (amniotic fluid). Polyhydramnios increases the risk of premature birth.Beginning in infancy, affected individuals often fail to ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  2. Chromosome 14 
    ... UPD 14. Maternal UPD 14 is associated with premature birth, slow growth before and after birth, short stature, ...
    https://medlineplus.gov/genetics/chromosome/14 - Genetics
  3. Trichothiodystrophy 
    ... Babies with trichothiodystrophy are at increased risk of premature birth, low birth weight, and slow growth. Most children ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  4. Tyrosinemia 
    ... C deficiency or an immature liver due to premature birth. Worldwide, tyrosinemia type I affects about 1 in ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
  5. CYB5R3 gene 
    ... to prevent chronic lung disease. The lungs of premature infants are often underdeveloped and need support after birth. Nitric oxide widens the blood vessels of the ...
    https://medlineplus.gov/genetics/gene/cyb5r3 - Genetics
  6. Gestational diabetes 
    ... associated high blood pressure (called preeclampsia) and early (premature) delivery of the baby.Babies of mothers with gestational diabetes tend to be large (macrosomia), which can cause complications during birth. Infants whose mothers have gestational diabetes are also ...
    https://medlineplus.gov/genetics/condition/gestational-diabetes - Genetics
  7. Gorlin-Chaudhry-Moss syndrome 
    ... and symptoms of this disorder are apparent from birth or infancy.Gorlin-Chaudhry-Moss syndrome is characterized by the premature closure of certain bones of the skull (craniosynostosis) ...
    https://medlineplus.gov/.../condition/gorlin-chaudhry-moss-syndrome - Genetics
  8. PDGFRB gene 
    ... disorders including infantile myofibromatosis; Kosaki overgrowth syndrome; and ... present at birth or in early infancy.Kosaki overgrowth syndrome is ...
    https://medlineplus.gov/genetics/gene/pdgfrb - Genetics
  9. WNT3 gene 
    ... one protein building block (amino acid) with a premature stop signal in the ... limb formation before birth and leads to the other serious birth defects ...
    https://medlineplus.gov/genetics/gene/wnt3 - Genetics
  10. 9q22.3 microdeletion 
    ... to unaffected peers. The macrosomia often begins before birth and continues into childhood. Other physical changes that are sometimes associated with a 9q22.3 microdeletion include the premature fusion of certain bones in the skull (metopic ...
    https://medlineplus.gov/genetics/condition/9q223-microdeletion - Genetics
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