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Bisalbuminemija kod bolesnika iz Hrvatske sa sarkoidozom
- Source :
- Biochemia Medica, Volume 19, Issue 1
- Publication Year :
- 2009
- Publisher :
- Medicinska naklada, 2009.
-
Abstract
- Uvod: Urođena bisalbuminemija je rijetka bolest, najčešće prisutna u benignom obliku, dosad opisivana u nekoliko patoloških stanja. Već su opisane dvije genske varijante kod dvije hrvatske obitelji. U ovom radu izvještavamo o novom slučaju bisalbuminemije kod bolesnika iz Hrvatske sa sarkoidozom. Metode: Bolesnik je, od strane liječnika opće prakse, upućen u KB „Sestre milosrdnice" na dijagnostički pregled pod sumnjom nasarkoidozu. Napravljena je kapilarna elektroforeza proteina u serumu s automatiziranim uređajem za kapilarnu elektroforezu. Rezultati: Temeljem laboratorijskih i patoloških nalaza potvrđena je sarkoidoza. Elektroforezom u serumu otkrivene su dvije različ ite frakcije albumina. Dodatna frakcija albumina bila je sporo migrirajuća. Ta sporo migrirajuća frakcija činila je 0,48, a normalna 0,51 ukupnog albumina. Sestra bolesnika također je imala bisalbuminemiju. Zaključak: Ovo je novi slučaj urođene bisalbuminemije kod bolesnika sa sarkoidozom. Ima li bisalbuminemija ikakve veze sa sarkoidozom, potrebno je tek razjasniti. Svaki slučaj pojave urođenih ili stečenih frakcija albumina trebao bi probuditi pažnju medicinskih biokemičara i kliničara, jer bi mogao pružiti uvid u evoluciju proteina kao i u fizičke, kemijske i molekularne karakteristike albumina.<br />Background: Inherited bisalbuminemia is rare, mostly benign state, which has so far been described in several pathological conditions. Two genetic variants have already been described in two Croatian families. Herein we report a new case of bisalbuminemia in a Croatian male patient with sarcoidosis. Methods: The patient was referred by a general practitioner to our hospital for a diagnostic work up for suspected sarcoidosis. Serum capillary protein electrophoresis was performed with automated capillary electrophoresis system. Results: Based on laboratory and pathologic findings, diagnosis of sarcoidosis was confirmed. Serum electrophoresis revealed two distinct albumin bands. Additional albumin variant was slow-migrating. The slow and a normal band made up for 0.48 and 0.51 of the total albumin, respectively. The patient's sister was also bisalbuminemic. Conclusions: This is a new case of inherited bisalbuminemia in a patient with sarcoidosis. Whether bisalbuminemia has any relevance to sarcoidosis, remains to be elucidated. Clinical chemists and clinicians should be alerted by every case of either inherited or acquired albumin variant, because it could provide insight into the protein evolution as well as the physical, chemical and molecular characteristics of albumin.
- Subjects :
- Pathology
medicine.medical_specialty
biology
business.industry
Genetic heterogeneity
Biochemistry (medical)
Clinical Biochemistry
Albumin
Serum albumin
bisalbuminemia
capillary zone electrophoresis
genetic heterogeneity
sarcoidosis
serum albumin
Gel electrophoresis of proteins
medicine.disease
Work-up
bisalbuminemija
kapilarna zonska elektroforeza
genetička heterogenost
sarkoidoza
albumin u serumu
biology.protein
Medicine
Sarcoidosis
business
Pathological
Bisalbuminemia
Subjects
Details
- Language :
- English
- ISSN :
- 18467482 and 13300962
- Volume :
- 19
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Biochemia Medica
- Accession number :
- edsair.doi.dedup.....b94e1a2ed3b69f7ada1220b471d6883d