Early Diagnosis of Fabry Disease in a Patient with Toe Tip Pain
Identifieur interne : 005939 ( Main/Exploration ); précédent : 005938; suivant : 005940Early Diagnosis of Fabry Disease in a Patient with Toe Tip Pain
Auteurs : Ki Bum Park [Corée du Sud] ; Kyung Ream Han [Corée du Sud] ; Jae Woo Lee [Corée du Sud] ; Seung Ho Kim [Corée du Sud] ; Do Wan Kim [Corée du Sud] ; Chan Kim [Corée du Sud] ; Jung Min Ko [Corée du Sud]Source :
- The Korean Journal of Pain [ 2005-9159 ] ; 2010.
Abstract
Fabry disease is an X-linked lysosomal disease caused by deficiency of α-galactosidase, in which early diagnosis may be missed due to the wide variety of clinical symptoms presenting during disease progression. A 13 year-old boy visited our pain clinic complaining of pricking and burning pain in the toe tips of both feet. Continuous epidural infusion for pain management was performed because of oral analgesics ineffectiveness. The patient underwent α-galactosidase A (GLA) enzyme analysis based on the clinical impression of Fabry disease from pain with a peripheral neuropathic component and history of anhidrosis. He was diagnosed with Fabry disease after confirming mutation of the GLA gene through a screening test of GLA activity. Enzyme replacement therapy was initiated and pain was tolerated with oral analgesics.
Url:
DOI: 10.3344/kjp.2010.23.3.207
PubMed: 20830268
PubMed Central: 2935984
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Fabry disease is an X-linked lysosomal disease caused by deficiency of α-galactosidase, in which early diagnosis may be missed due to the wide variety of clinical symptoms presenting during disease progression. A 13 year-old boy visited our pain clinic complaining of pricking and burning pain in the toe tips of both feet. Continuous epidural infusion for pain management was performed because of oral analgesics ineffectiveness. The patient underwent α-galactosidase A (GLA) enzyme analysis based on the clinical impression of Fabry disease from pain with a peripheral neuropathic component and history of anhidrosis. He was diagnosed with Fabry disease after confirming mutation of the GLA gene through a screening test of GLA activity. Enzyme replacement therapy was initiated and pain was tolerated with oral analgesics.</p>
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<affiliations><list><country><li>Corée du Sud</li>
</country>
<region><li>Région capitale de Séoul</li>
</region>
<settlement><li>Séoul</li>
</settlement>
</list>
<tree><country name="Corée du Sud"><noRegion><name sortKey="Park, Ki Bum" sort="Park, Ki Bum" uniqKey="Park K" first="Ki Bum" last="Park">Ki Bum Park</name>
</noRegion>
<name sortKey="Han, Kyung Ream" sort="Han, Kyung Ream" uniqKey="Han K" first="Kyung Ream" last="Han">Kyung Ream Han</name>
<name sortKey="Kim, Chan" sort="Kim, Chan" uniqKey="Kim C" first="Chan" last="Kim">Chan Kim</name>
<name sortKey="Kim, Do Wan" sort="Kim, Do Wan" uniqKey="Kim D" first="Do Wan" last="Kim">Do Wan Kim</name>
<name sortKey="Kim, Seung Ho" sort="Kim, Seung Ho" uniqKey="Kim S" first="Seung Ho" last="Kim">Seung Ho Kim</name>
<name sortKey="Ko, Jung Min" sort="Ko, Jung Min" uniqKey="Ko J" first="Jung Min" last="Ko">Jung Min Ko</name>
<name sortKey="Lee, Jae Woo" sort="Lee, Jae Woo" uniqKey="Lee J" first="Jae Woo" last="Lee">Jae Woo Lee</name>
</country>
</tree>
</affiliations>
</record>
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