Neonatal jaundice history and symptoms: Difference between revisions
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==History== | ==History== | ||
==Symptoms== | * Family and maternal history is important for diagnosing neonatal jaundice and the management approach. | ||
* For the family history, the following should be evaluated: | |||
** History of previous sibling developed neonatal jaundice | |||
** Family history of jaundice | |||
** Family history of anemia or hereditary hemolytic disorders | |||
** Family members with liver disease | |||
* For the maternal history, the following should be evaluated: | |||
** The history of pregnancy and delivery | |||
** Any maternal complications or illness during the pregnancy | |||
** Breastfeeding history | |||
** Usage of any drugs | |||
==Symptoms== | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} |
Revision as of 20:50, 7 January 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
History
- Family and maternal history is important for diagnosing neonatal jaundice and the management approach.
- For the family history, the following should be evaluated:
- History of previous sibling developed neonatal jaundice
- Family history of jaundice
- Family history of anemia or hereditary hemolytic disorders
- Family members with liver disease
- For the maternal history, the following should be evaluated:
- The history of pregnancy and delivery
- Any maternal complications or illness during the pregnancy
- Breastfeeding history
- Usage of any drugs