Please use this identifier to cite or link to this item:
http://repo.knmu.edu.ua/handle/123456789/7375Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Vasylieva, Oksana | - |
| dc.contributor.author | Katsapov, Dmytro | - |
| dc.date.accessioned | 2014-11-05T13:52:48Z | - |
| dc.date.available | 2014-11-05T13:52:48Z | - |
| dc.date.issued | 2014 | - |
| dc.identifier.citation | Vasylieva O. V. The diagnostics case of Familial Mediterranean fever occured under the chronic pancreatitis mask / O. V. Vasylieva, D. V. Katsapov // Journal of Inherited Metabolic Disease. – 2014. – Vol. 37, suppl. 1 : Annual Sympozium for the Stady of Inbirn Errors of Metabolist, Innsbruck, Austria, 2–5 September, 2014. – P. 184–185. | uk_UA |
| dc.identifier.uri | https://repo.knmu.edu.ua/handle/123456789/7375 | - |
| dc.description | The patient is heterozygote compaund for the mutations M694I and M694V in exon 10 MEFV. FMF was diagnosed in this case, which was occuring with symptoms of chronic pancreatitis. It is known that the severity of clinical signs can be decreased in heterozygous carriers of mutant alleles. However, given the possibility of FMF-associated amyloidosis, rheumatologist clinical supervision and control of serum amyloid were recommended. | uk_UA |
| dc.description.abstract | Familial Mediterranean fever (FMF) is the most common hereditary periodic fever syndrome, which affecting populations of Mediterranean origin (Arabs, Turks, Jews, Lebanese, Greeks, etc.). The frequency of heterozygous carriers of MEFV, responsible for the development of FMF, is more than 1/5 of the total population. | uk_UA |
| dc.language.iso | en | uk_UA |
| dc.subject | fever | uk_UA |
| dc.subject | mediterranean | uk_UA |
| dc.subject | molecular genetic testing | uk_UA |
| dc.title | The diagnostics case of Familial Mediterranean fever occured under the chronic pancreatitis mask | uk_UA |
| dc.type | Thesis | uk_UA |
| Appears in Collections: | Наукові праці. Кафедра фізіології | |
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