Differentiating Galactosemia from other diseases: Difference between revisions
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| [[Glucose-6-phosphate]] [[dehydrogenase]] [[deficiency]] || Example || Example || Example || Example | | [[Glucose-6-phosphate]] [[dehydrogenase]] [[deficiency]] || Example || Example || Example || Example | ||
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==References== | ==References== | ||
Revision as of 21:48, 27 May 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]
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Overview
Differentiating Galactosemia from other Diseases
Galactosemia needs to differentiated from other diseases like:
References
- ↑ Sakura N, Mizoguchi N, Ono H, Yamaoka H, Hamakawa M (2000). "Congenital biliary atresia detected as a result of galactosemia screening by the Beutler method". Clin Chim Acta. 298 (1–2): 175–9. doi:10.1016/s0009-8981(00)00220-5. PMID 10876013.
- ↑ Müller D, Santer R, Krawinkel M, Christiansen B, Schaub J (1997). "Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia". J Inherit Metab Dis. 20 (4): 607–8. doi:10.1023/a:1005375629820. PMID 9266402.
- ↑ Stuhrman G, Perez Juanazo SJ, Crivelly K, Smith J, Andersson H, Morava E (2017). "False-Positive Newborn Screen Using the Beutler Spot Assay for Galactosemia in Glucose-6-Phosphate Dehydrogenase Deficiency". JIMD Rep. 36: 1–5. doi:10.1007/8904_2016_34. PMC 5680284. PMID 28078493.
| Diseases | Clinical manifestations | Para-clinical findings | Gold standard | Additional findings |
|---|---|---|---|---|
| Galactosemia | Example | Example | Example | Example |
| Biliary atresia | Example | Example | Example | Example |
| Fanconi Bickel syndrome | Example | Example | Example | Example |
| Glucose-6-phosphate dehydrogenase deficiency | Example | Example | Example | Example |