Znanstveni rad - Pregledni rad
Insights into complexity of congenital disorders of glycosylation

Supraha Goreta, Sandra; Dabelic, Sanja; Dumic, Jerka (2012)
Podaci o radu
Jezik rada engleski
Naslov (engleski)Insights into complexity of congenital disorders of glycosylation
AutorSupraha Goreta, Sandra
Dabelic, Sanja
Dumic, Jerka
Sažetak rada (engleski)
Biochemical and biological properties of glycoconjugates are strongly determined by the specific structure of its glycan parts. Glycosylation, the covalent attachment of sugars to proteins and lipids, is very complex and highly-coordinated process involving > 250 gene products. Deficiency of glycosylation enzymes or transporters results in impaired glycosylation, and consequently pathologi-cal modulation of many physiological processes. Inborn defects of glycosylation enzymes, caused by the specific mutations, lead to the development of rare, but severe diseases – congenital disorders of glycosylation (CDGs). Up today, there are more than 45 known CDGs. Their clinical manifestations range from very mild to extremely severe (even lethal) and unfortunately, only three of them can be effectively treated nowadays. CDG symptoms highly vary, though some are common for several CDG types but also for other unrelated diseases, especially neurological ones, leaving the possibility that many CDGs cases are under- or misdiagnosed. Glycan analysis of serum transferrin (by isoelectric focusing or more sophisticated methods, such as HPLC (high-performance liquid chromatography) or MALDI (matrix-assisted laser desorption/ionization)) or serum N-glycans (by MS), enzyme activity assays and DNA sequence analysis are the most frequently used methods for CDG screening and identification, since no specific tests are available yet. In this review we summarize the current knowledge on the clinical, biochemical and genetic characteristic of distinct CDGs, as well as existing diagnostic and therapeutic procedures, aiming to contribute to the awareness on the existence of the-se rare diseases and encourage the efforts to elucidate its genetic background, improve diagnostics and develop new strategies for their treatment.
Ključne riječi (engleski)congenital disorders of glycosylation CDG diagnostics therapy
Vrsta radaznanstveni rad - pregledni rad
Status objave radaobjavljen
Vrsta recenzijerecenziran
Naslov časopisaBiochemia medica : Biochemia medica
Brojčani podaci2012, Vol. 22, br. 2, str. 156-170
ISSN1330-0962
Datumdatum objave publikacije: 15.06.2012.
URL radahttp://hrcak.srce.hr/83220
Znanstveno područjeBIOMEDICINA I ZDRAVSTVO
Farmacija
Medicinska biokemija
UstanovaSveučilište u Zagrebu, Farmaceutsko-biokemijski fakultet
URN:NBNhttps://urn.nsk.hr/urn:nbn:hr:163:176390