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30 Cards in this Set
- Front
- Back
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herniation of the intestines within a peritoneal sac
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omphacele
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upward slanted palpebral fissures
epicanthal folds single simean crease |
trisomy 21
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GI disorders present in trisomy 21
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duodenal atresia
Hirschsprung disease tracheoesophageal fistula |
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GI condition assx with trisomy 13
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omphacele
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GI condition assx with trisomy 18
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omphacele
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delayed passage of stool at birth
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hirschsprung disease
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bile stained emesis
no audible bowel sounds |
malrotation with volvulus
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conditions assx with bilious emesis
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malrotation w/ volvulus
duodenal atresia |
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double bubble sign on x ray
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intestinal atresia
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inheritance pattern of FAP
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autosomal dominant
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onset of sx with FAP
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8 years
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Gardner syndrome
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variant of FAP with multiple osteomas
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normal liver uptake of bile, but absent excretion into the bowel
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biliary atresia
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type of bilirubin that builds up in biliary atresia
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direct
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hepatomegaly
cataracts mental retardation |
galactosemia
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tx of galactosemia
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removal of galactose from the diet (animal milks)
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disease with absent bilirubin UGT
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Criger Najjar syndrome type I
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currant jelly stools
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HSP
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colicky abdominal pain
tea colored urine palpable rash |
HSP
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term for bloody stools
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hematochezia
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where does intussesception usually take place
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lead points (meckel diverticulum, intestinal polyps, neurofibroma)
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projectile vomiting
small mass in epigastrum |
pyloric stenosis
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lab values in pyloric stenosis
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metabolic alkalosis
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baby feeds eagerly, immediately vomits, and is ready to eat again
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pyloric stenosis
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feeding intolerance
hematochezia first 2 weeks of life |
NEC (necrotizing enterocolitis)
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poor weight gain
diarrhea flatulence rice and milk do not cause sx |
celiac sprue
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things that are tolerable in celiac sprue
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corn and rice
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things that are intolerable in celiac sprue
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wheat, oat, barley, or rye
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UGT activity blocked by breast milk
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breast milk jaundice
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decreased activity of UGT
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physiologic jaundice
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