Galactosemia history and symptoms: Difference between revisions
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==Overview== | ==Overview== | ||
==History== | ==History== | ||
[[Galactosemia]] is manifested mostly in the first week of life. Hence, [[diagnosis]] is mainly [[clinical]] and by [[newborn]] [[screening]], some being detected occasionally by [[family]] [[history]].<ref name="pmid263527">{{cite journal| author=Bozkowa K, Zbieg-Sendecka E, Grodzka Z, Cabalska B| title=[Clinical and biochemical diagnosis of galactosemia among our cases]. | journal=Probl Med Wieku Rozwoj | year= 1979 | volume= 8 | issue= | pages= 63-9 | pmid=263527 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=263527 }} </ref> | |||
==Symptoms== | ==Symptoms== |
Revision as of 12:02, 4 July 2022
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Dayana Davidis, M.D. [2]
Overview
History
Galactosemia is manifested mostly in the first week of life. Hence, diagnosis is mainly clinical and by newborn screening, some being detected occasionally by family history.[1]
Symptoms
References
- ↑ Bozkowa K, Zbieg-Sendecka E, Grodzka Z, Cabalska B (1979). "[Clinical and biochemical diagnosis of galactosemia among our cases]". Probl Med Wieku Rozwoj. 8: 63–9. PMID 263527.