Fabry's disease differential diagnosis: Difference between revisions
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!Fabry's disease | |||
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| rowspan=" | | rowspan="3" |Skin | ||
| rowspan=" | | rowspan="3" |Angiokeratoma<br /> | ||
|[[Fucosidosis]] | | rowspan="3" | | ||
* Mean age: 17 years | |||
* Locations: Mostly [[Hip (anatomy)|Hips]], [[Groin area|Groin]], [[Periumbilical]] | |||
|[[Fucosidosis]]<ref name="pmid33266441">{{cite journal| author=Stepien KM, Ciara E, Jezela-Stanek A| title=Fucosidosis-Clinical Manifestation, Long-Term Outcomes, and Genetic Profile-Review and Case Series. | journal=Genes (Basel) | year= 2020 | volume= 11 | issue= 11 | pages= | pmid=33266441 | doi=10.3390/genes11111383 | pmc=7700486 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=33266441 }}</ref> | |||
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* | *Mean age: 2 years, the older patients more likely to have in examination | ||
*Location: Varies involve Hips, Groin, Abdomen, external genitalia | |||
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*The clinical appearance of the lesions may be indistinguishable. | |||
*The light microscopic findings are indistinguishable. | *The light microscopic findings are indistinguishable. | ||
*Should Investigate accompanying symptoms | |||
< | |- | ||
|[[Sialidosis]] (Juvenile foem)<ref name="pmid22452439">{{cite journal| author=Zampetti A, Orteu CH, Antuzzi D, Bongiorno MR, Manco S, Gnarra M | display-authors=etal| title=Angiokeratoma: decision-making aid for the diagnosis of Fabry disease. | journal=Br J Dermatol | year= 2012 | volume= 166 | issue= 4 | pages= 712-20 | pmid=22452439 | doi=10.1111/j.1365-2133.2012.10742.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22452439 }}</ref> | |||
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* Mean age : 2 years | |||
* Location: Diffuse | |||
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* The clinical appearance of the lesions may be indistinguishable. | |||
* Should Investigate accompanying symptoms | |||
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|[[Acral pseudolymphomatous]] angiokeratoma of childhood<ref name="pmid20465644">{{cite journal| author=Chedraoui A, Malek J, Tamraz H, Zaynoun S, Kibbi AG, Ghosn S| title=Acral pseudolymphomatous angiokeratoma of children in an elderly man: report of a case and review of the literature. | journal=Int J Dermatol | year= 2010 | volume= 49 | issue= 2 | pages= 184-8 | pmid=20465644 | doi=10.1111/j.1365-4632.2009.04203.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20465644 }}</ref> | |||
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* Mainly children | |||
* Location: Trunk and exterimities | |||
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*Investigate accompanying symptoms | * Should Investigate accompanying symptoms | ||
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Revision as of 20:19, 13 March 2022
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Fabry's disease Microchapters |
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Diagnosis |
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Treatment |
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Fabry's disease differential diagnosis On the Web |
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American Roentgen Ray Society Images of Fabry's disease differential diagnosis |
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Risk calculators and risk factors for Fabry's disease differential diagnosis |
Differentiating Fabry's disease from other disease
| Fabry's disease | |||||
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| Skin | Angiokeratoma |
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Fucosidosis[1] |
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| Sialidosis (Juvenile foem)[2] |
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| Acral pseudolymphomatous angiokeratoma of childhood[3] |
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References
- ↑ Stepien KM, Ciara E, Jezela-Stanek A (2020). "Fucosidosis-Clinical Manifestation, Long-Term Outcomes, and Genetic Profile-Review and Case Series". Genes (Basel). 11 (11). doi:10.3390/genes11111383. PMC 7700486 Check
|pmc=value (help). PMID 33266441 Check|pmid=value (help). - ↑ Zampetti A, Orteu CH, Antuzzi D, Bongiorno MR, Manco S, Gnarra M; et al. (2012). "Angiokeratoma: decision-making aid for the diagnosis of Fabry disease". Br J Dermatol. 166 (4): 712–20. doi:10.1111/j.1365-2133.2012.10742.x. PMID 22452439.
- ↑ Chedraoui A, Malek J, Tamraz H, Zaynoun S, Kibbi AG, Ghosn S (2010). "Acral pseudolymphomatous angiokeratoma of children in an elderly man: report of a case and review of the literature". Int J Dermatol. 49 (2): 184–8. doi:10.1111/j.1365-4632.2009.04203.x. PMID 20465644.