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Results 1 - 10 of 12 for Feeding difficulties
  1. MCEE gene 
    ... to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, and long-term health problems. These ...
    https://medlineplus.gov/genetics/gene/mcee - Genetics
  2. TSPYL1 gene 
    ... problems, a slow or uneven heart rate, and feeding difficulties.The mutation that causes SIDDT inserts a single ...
    https://medlineplus.gov/genetics/gene/tspyl1 - Genetics
  3. MMADHC gene 
    ... to cause methylmalonic acidemia, a condition characterized by feeding difficulties, life-threatening episodes of low blood glucose and ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  4. MMUT gene 
    ... people with methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, and long-term health problems. These ...
    https://medlineplus.gov/genetics/gene/mmut - Genetics
  5. MMAB gene 
    ... to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, and long-term health problems. Some ...
    https://medlineplus.gov/genetics/gene/mmab - Genetics
  6. MMAA gene 
    ... to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, and long term health problems. Some ...
    https://medlineplus.gov/genetics/gene/mmaa - Genetics
  7. HADHB gene 
    ... of mitochondrial trifunctional protein deficiency. These features include feeding difficulties, lethargy, hypoglycemia, weak muscle tone (hypotonia), and liver ...
    https://medlineplus.gov/genetics/gene/hadhb - Genetics
  8. OPA1 gene 
    ... the limbs (peripheral neuropathy), difficulty coordinating movements (ataxia), feeding and digestive difficulties, and developmental delay. The features of these conditions ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  9. SLC25A15 gene 
    ... blood. This condition can cause extreme tiredness (lethargy), difficulty feeding, problems controlling breathing or body temperature, and seizures in infancy. Affected adults can have episodes of vomiting, difficulty with movements, liver problems, or neurological problems.The ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics
  10. HLCS gene 
    ... to use biotin effectively. Affected infants often have difficulty feeding, breathing problems, a skin rash, hair loss (alopecia), ...
    https://medlineplus.gov/genetics/gene/hlcs - Genetics
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