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Results 1 - 9 of 9 for Congenital short bowel syndrome
  1. Intestinal pseudo-obstruction 
    ... condition. Chronic idiopathic intestinal pseudo-obstruction CIIP CIPO Congenital short bowel syndrome Enteric neuropathy Familial visceral myopathy Familial visceral neuropathy ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  2. Abdominal wall defect 
    ... loss of intestinal tissue, and a condition called short bowel syndrome that occurs when areas of the small intestine ...
    https://medlineplus.gov/genetics/condition/abdominal-wall-defect - Genetics
  3. Hirschsprung disease 
    ... or from all of the large and small intestine (total intestinal aganglionosis).Hirschsprung disease can occur in combination with other conditions, such as Waardenburg syndrome, type IV; Mowat-Wilson syndrome; or congenital central hypoventilation syndrome. These cases are described as ...
    https://medlineplus.gov/genetics/condition/hirschsprung-disease - Genetics
  4. Pallister-Killian mosaic syndrome 
    ... percent of affected infants are born with a congenital diaphragmatic hernia, which ... mosaic syndrome vary, although most people with this disorder have ...
    https://medlineplus.gov/.../pallister-killian-mosaic-syndrome - Genetics
  5. Donnai-Barrow syndrome 
    ... disability and developmental delay.People with Donnai-Barrow syndrome may also ... the stomach and intestines to move into the chest and possibly crowd ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  6. Fryns syndrome 
    ... the diaphragm). The most common defect is a congenital diaphragmatic hernia, ... with Fryns syndrome typically have abnormalities of the fingers and toes ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
  7. L1CAM gene 
    ... function of nerve cells in the brain and intestine, leading to hydrocephalus and Hirschsprung disease. ... Christaller WA, Vos Y, Gebre-Medhin S, Hofstra RM, Schafer MK. L1 syndrome diagnosis complemented with functional analysis of L1CAM variants ...
    https://medlineplus.gov/genetics/gene/l1cam - Genetics
  8. Down syndrome 
    ... point upward (upslanting palpebral fissures), small ears, a short neck, and a ... of the intestine, are less common.Individuals with Down syndrome have ...
    https://medlineplus.gov/genetics/condition/down-syndrome - Genetics
  9. Myhre syndrome 
    ... with age.Common signs and symptoms of Myhre syndrome include short stature, skeletal abnormalities, limited joint mobility, characteristic facial ... inherits the mutation from one affected parent. LAPS syndrome Laryngotracheal stenosis, arthropathy, prognathism, and ... Genetic Testing Registry: Myhre syndrome Myhre syndrome ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics