Abstract | AIM: To characterize patients with various nosological unities [symbol: see text] of porphyria in accordance with their age, clinical symptoms, provoking factors, therapy and outcome. MATERIAL AND METHODS: RESULTS: The patients were from the CIS. The overwhelming majority of them were young and middle-aged subjects. Rapid development of the disease and severe neurological symptoms were predominantly observed in patients with acute forms of porphyria. CONCLUSION: Early diagnosis of porphyrin metabolism disorders makes it possible to decrease abruptly the number of cases leading to severe complications, disability, and fatal outcome. The use of inexpensive methods of screening of porphyrin metabolism disorders provides a promising approach to solving this problem. These methods should be used in municipal hospitals. In addition, asymptomatic carriers of defective gene should be revealed at the preclinical stage using various methods of molecular genetic assay.
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Authors | Ia S Pustovoĭt, I V Karpova, A V Pivnik, V L Surin, A V Luk'ianenko, Iu A Luchinina |
Journal | Terapevticheskii arkhiv
(Ter Arkh)
Vol. 75
Issue 7
Pg. 68-73
( 2003)
ISSN: 0040-3660 [Print] Russia (Federation) |
Vernacular Title | Klinicheskie proiavleniia narusheniĭ porfirinovogo obmena. |
PMID | 12934485
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Porphyrins
- Heme
- Inosine Diphosphate
- Arginine
- heme arginate
- Octreotide
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Topics |
- Acute Disease
- Adolescent
- Adult
- Arginine
(therapeutic use)
- Chronic Disease
- Female
- Heme
(therapeutic use)
- Humans
- Inosine Diphosphate
(therapeutic use)
- Middle Aged
- Octreotide
(therapeutic use)
- Plasmapheresis
- Porphyria, Acute Intermittent
(diagnosis, drug therapy, etiology, metabolism)
- Porphyria, Erythropoietic
(diagnosis, drug therapy, etiology, metabolism)
- Porphyrias
(diagnosis, drug therapy, etiology, metabolism)
- Porphyrins
(metabolism)
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