Fabry's disease laboratory findings: Difference between revisions

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==Laboratory Findings==
==Laboratory Findings==
*Blood tests
*Blood tests
**[[Anemia]]  
**[[Anemia]]
**[[Serum creatinine]] may be raised from [[chronic renal failure]]
**[[Serum creatinine]] may be raised from [[chronic renal failure]]
**Serum [[urea]] may be elevated
**Serum [[urea]] may be elevated
**[[BUN]] may be raised
**[[BUN]] may be raised
**Electrolyte disturbance maybe presented due to renal failure
*[[Urinalysis]]:
*[[Urinalysis]]:
**[[Hematuria]]
**[[Hematuria]]
**[[Proteinuria]]
**[[Proteinuria]]
**Mulberry bodies [distal epithelial cell+ [[Globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase|globotriaosylceramide]] accumulation]
*[[Enzymatic]] analysis
**Drop activity of Alpha-galactosidase A activity [in male (hemizygote) patients, is not reliable in female and heterozygotes] 
*Elevated of [[Gb3]] concentration in plasma or leukocytes
== Genetic Testing ==
* Detection of GLA gene mutation [ After Alpha-galactosidase A activity in male patients, First place after suspected in females]


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 18:26, 9 April 2022

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Laboratory Findings

Genetic Testing

  • Detection of GLA gene mutation [ After Alpha-galactosidase A activity in male patients, First place after suspected in females]

References