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Results 1 - 10 of 80 for Feeding difficulties in infancy
  1. Tetrasomy 18p 
    ... parts of the body. This condition usually causes feeding difficulties in infancy, delayed development, intellectual disability that is often mild to moderate but can be severe, changes in muscle tone, distinctive facial ... have trouble feeding and may vomit frequently, which makes it difficult ...
    https://medlineplus.gov/genetics/condition/tetrasomy-18p - Genetics
  2. ADNP syndrome 
    ... ADNP syndrome have weak muscle tone (hypotonia) and feeding difficulties in infancy. They may also have digestive system problems, such ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
  3. Jacobsen syndrome 
    ... side of the heart (hypoplastic left heart syndrome); feeding difficulties in infancy; short stature; frequent ear and sinus infections; and ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  4. MECP2 duplication syndrome 
    ... this condition also have weak muscle tone in infancy, feeding difficulties, poor or absent speech, or muscle stiffness (rigidity). ...
    https://medlineplus.gov/.../condition/mecp2-duplication-syndrome - Genetics
  5. Mitochondrial trifunctional protein deficiency 
    ... or later in life. Features that occur during infancy include feeding difficulties, lack of energy (lethargy), low blood glucose (hypoglycemia), weak muscle tone (hypotonia), and liver problems. Infants with this ... begin after infancy include hypotonia, muscle pain, a breakdown of muscle ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  6. Cap myopathy 
    ... can worsen over time.Affected individuals may have feeding and swallowing difficulties in infancy. They typically have delayed development of motor skills ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
  7. STAC3 disorder 
    ... features of STAC3 disorder. Affected individuals may have feeding and swallowing difficulties in infancy. They usually have delayed development of motor skills ...
    https://medlineplus.gov/genetics/condition/stac3-disorder - Genetics
  8. Goldenhar Syndrome (For Parents) (Nemours Foundation)  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Nemours Foundation ... Goldenhar Syndrome, cleft and craniofacial, clefts, craniofacial, birth ...
    https://kidshealth.org/en/parents/goldenhar-syndrome.html - External Health Links
  9. Spastic paraplegia type 49 
    ... of spastic paraplegia type 49. Affected individuals have difficulty feeding beginning in infancy. They experience a backflow of stomach acids into ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-49 - Genetics
  10. SATB2-associated syndrome 
    ... SATB2-associated syndrome. Less common neurological problems include feeding difficulties and weak muscle tone (hypotonia) in infancy. About half of affected individuals have abnormalities in ...
    https://medlineplus.gov/genetics/condition/satb2-associated-syndrome - Genetics
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