Galactosemia natural history, complications and prognosis: Difference between revisions
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{{CMG}} {{AE}} {{Sujaya}} | {{CMG}} {{AE}} {{Sujaya}} | ||
[[Acute]] [[neonatal]] [[illness]] is experienced by most patients. [[Clinical]] [[features]] include <ref name="pmid31029175">{{cite journal| author=Rubio-Gozalbo ME, Haskovic M, Bosch AM, Burnyte B, Coelho AI, Cassiman D | display-authors=etal| title=The natural history of classic galactosemia: lessons from the GalNet registry. | journal=Orphanet J Rare Dis | year= 2019 | volume= 14 | issue= 1 | pages= 86 | pmid=31029175 | doi=10.1186/s13023-019-1047-z | pmc=6486996 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31029175 }} </ref> having one or more of: | [[Acute]] [[neonatal]] [[illness]] is experienced by most patients. A reported lower [[enzyme]] activity leads to more severe presentation while [[newborn]] [[screening]] results in detection at more favorable stages of the [[disease]]. [[Clinical]] [[features]] include <ref name="pmid31029175">{{cite journal| author=Rubio-Gozalbo ME, Haskovic M, Bosch AM, Burnyte B, Coelho AI, Cassiman D | display-authors=etal| title=The natural history of classic galactosemia: lessons from the GalNet registry. | journal=Orphanet J Rare Dis | year= 2019 | volume= 14 | issue= 1 | pages= 86 | pmid=31029175 | doi=10.1186/s13023-019-1047-z | pmc=6486996 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31029175 }} </ref> having one or more of: | ||
* Elevated [[liver]] [[enzymes]] | * Elevated [[liver]] [[enzymes]] | ||
* [[Hypoglycemia]] | * [[Hypoglycemia]] | ||
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* [[Sepsis]] | * [[Sepsis]] | ||
* [[Bleeding]] [[diathesis]] | * [[Bleeding]] [[diathesis]] | ||
A younger age of [[diagnosis]] and early introduction of [[dietary]] changes exert a positive effect on the natural history of [[galactosemia]] <ref name="pmid9266215">{{cite journal| author=Berry GT, Nissim I, Gibson JB, Mazur AT, Lin Z, Elsas LJ | display-authors=etal| title=Quantitative assessment of whole body galactose metabolism in galactosemic patients. | journal=Eur J Pediatr | year= 1997 | volume= 156 Suppl 1 | issue= | pages= S43-9 | pmid=9266215 | doi=10.1007/pl00014271 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9266215 }} </ref> <ref name="pmid22483615">{{cite journal| author=Berry GT| title=Galactosemia: when is it a newborn screening emergency? | journal=Mol Genet Metab | year= 2012 | volume= 106 | issue= 1 | pages= 7-11 | pmid=22483615 | doi=10.1016/j.ymgme.2012.03.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22483615 }} </ref>. | |||
==Complications== | ==Complications== | ||
Revision as of 09:10, 3 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
The only scientifically approved and effective treatment for classic galactosemia is eliminating galactose from the diet, through elimination of dairy products. Individuals with Duarte variant of galactosemia do not need to eliminate galactose from their diet at all and may not experience any symptoms. However, even with an early diagnosis and subsequent elimination of galactose from the diet, some individuals diagnosed with classic galactosemia experience long term complications such as speech difficulties, learning disabilities and neurological impairment. Newborns with classic galactosemia will show symptoms the first days of life if they are fed formula or breast milk which contain lactose. They will develop symptoms like convulsions, irritability, lethargy, poor appetite and baby refusing to be fed, poor weight gain, vomiting and jaundice noticed with yellow skin and yellow whites of the eyes.
Natural History
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3] Associate Editor(s)-in-Chief: Sujaya Chattopadhyay, M.D.[4]
Acute neonatal illness is experienced by most patients. A reported lower enzyme activity leads to more severe presentation while newborn screening results in detection at more favorable stages of the disease. Clinical features include [1] having one or more of:
A younger age of diagnosis and early introduction of dietary changes exert a positive effect on the natural history of galactosemia [2] [3].
Complications
Prognosis
References
- ↑ Rubio-Gozalbo ME, Haskovic M, Bosch AM, Burnyte B, Coelho AI, Cassiman D; et al. (2019). "The natural history of classic galactosemia: lessons from the GalNet registry". Orphanet J Rare Dis. 14 (1): 86. doi:10.1186/s13023-019-1047-z. PMC 6486996. PMID 31029175.
- ↑ Berry GT, Nissim I, Gibson JB, Mazur AT, Lin Z, Elsas LJ; et al. (1997). "Quantitative assessment of whole body galactose metabolism in galactosemic patients". Eur J Pediatr. 156 Suppl 1: S43–9. doi:10.1007/pl00014271. PMID 9266215.
- ↑ Berry GT (2012). "Galactosemia: when is it a newborn screening emergency?". Mol Genet Metab. 106 (1): 7–11. doi:10.1016/j.ymgme.2012.03.007. PMID 22483615.