Template:Neonatal jaundice differential diagnosis - Revision history

ClaireLewis at 19:39, 29 September 2019

2019-09-29T19:39:33Z

← Revisión anterior		Revisión del 19:39 29 sep 2019
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	**Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.		**Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.
	*Blood group incompatibility: ABO, Rh factor, minor antigens		*Blood group incompatibility: ABO, Rh factor, minor antigens
	*[[Diabetic mother]]/gestational diabetes		*[[DM\|Diabetic mother]]/gestational diabetes
	*Internal [[hemorrhage]]		*Internal [[hemorrhage]]
	*Physiologic jaundice		*Physiologic jaundice
Línea 25:		Línea 25:
	*[[Cytomegalovirus]] infection		*[[Cytomegalovirus]] infection
	*[[Sepsis]]		*[[Sepsis]]
	*TORCH infection		*TORCH infection ([[toxoplasma]], other/[[syphilis]], [[rubella]], [[CMV]], [[HSV]])
	*[[Biliary atresia]]		*[[Biliary atresia]]
	*[[Cystic fibrosis]]		*[[Cystic fibrosis]]
	*Hepatic infarction		*Hepatic infarction
	*[[Inborn errors of metabolism]] (e.g., galactosemia, tyrosinosis)		*[[Inborn errors of metabolism]] (e.g., galactosemia, tyrosinosis)

ClaireLewis at 19:37, 29 September 2019

2019-09-29T19:37:13Z

← Revisión anterior		Revisión del 19:37 29 sep 2019
Línea 7:		Línea 7:
	**Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.		**Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.
	*Blood group incompatibility: ABO, Rh factor, minor antigens		*Blood group incompatibility: ABO, Rh factor, minor antigens
	*Diabetic mother/gestational diabetes		*[[Diabetic mother]]/gestational diabetes
	*Internal hemorrhage		*Internal [[hemorrhage]]
	*Physiologic jaundice		*Physiologic jaundice
	*Polycythemia		*[[Polycythemia]]
	*[[Sepsis]]		*[[Sepsis]]
	*Hemoglobinopathies: thalassemia		*Hemoglobinopathies: [[thalassemia]]
	*Red blood cell enzyme defects: [[G6PD Deficiency]], pyruvate kinase		*Red blood cell enzyme defects: [[G6PD Deficiency]], pyruvate kinase
	*Red blood cell membrane disorders: spherocytosis, ovalocytosis		*Red blood cell membrane disorders: spherocytosis, ovalocytosis
	*Hypothyroidism		*[[Hypothyroidism]]
	*[[Immune thrombocytopenic purpura]]		*[[Immune thrombocytopenic purpura]]
	*Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)		*Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)
Línea 23:		Línea 23:
	*Hyperalimentation cholestasis		*Hyperalimentation cholestasis
	*Neonatal [[hepatitis]]		*Neonatal [[hepatitis]]
	*Cytomegalovirus infection		*[[Cytomegalovirus]] infection
	*[[Sepsis]]		*[[Sepsis]]
	*TORCH infection		*TORCH infection
	*Biliary atresia		*[[Biliary atresia]]
	*Cystic fibrosis		*[[Cystic fibrosis]]
	*Hepatic infarction		*Hepatic infarction
	*Inborn errors of metabolism (e.g., galactosemia, tyrosinosis)		*[[Inborn errors of metabolism]] (e.g., galactosemia, tyrosinosis)

Ostermayer at 21:29, 25 October 2016

2016-10-25T21:29:51Z

← Revisión anterior		Revisión del 21:29 25 oct 2016
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	*[[Immune thrombocytopenic purpura]]		*[[Immune thrombocytopenic purpura]]
	*Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)		*Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)


	===Direct (Conjugated) Hyperbilirubinemia===		===Direct (Conjugated) Hyperbilirubinemia===

Ostermayer: Created page with " ===Indirect (Unconjugated) Hyperbilirubinemia=== ''More common causes are listed first, followed by less common causes *Breast milk jaundice **Due to substances in milk t..."

2016-10-25T21:28:40Z

Created page with " ===Indirect (Unconjugated) Hyperbilirubinemia=== ''More common causes are listed first, followed by less common causes *Breast milk jaundice **Due to substances in milk t..."

Página nueva

===Indirect (Unconjugated) Hyperbilirubinemia===
''More common causes are listed first, followed by less common causes
*[[Breast milk jaundice]]
**Due to substances in milk that inhibits glucuronyl transferase. It may start as early as 3rd day and reaches peak by 3rd week of life. It is unlikely to cause kernicterus
*[[Breast feeding jaundice]]
**Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.
*Blood group incompatibility: ABO, Rh factor, minor antigens
*Diabetic mother/gestational diabetes
*Internal hemorrhage
*Physiologic jaundice
*Polycythemia
*[[Sepsis]]
*Hemoglobinopathies: thalassemia
*Red blood cell enzyme defects: [[G6PD Deficiency]], pyruvate kinase
*Red blood cell membrane disorders: spherocytosis, ovalocytosis
*Hypothyroidism
*[[Immune thrombocytopenic purpura]]
*Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)

===Direct (Conjugated) Hyperbilirubinemia===
''Conjugated bilirubinemia implies a hepatic or post hepatic cause. More common causes are listed first.
*Hyperalimentation cholestasis
*Neonatal [[hepatitis]]
*Cytomegalovirus infection
*[[Sepsis]]
*TORCH infection
*Biliary atresia
*Cystic fibrosis
*Hepatic infarction
*Inborn errors of metabolism (e.g., galactosemia, tyrosinosis)