Author/Editor		Lužnik-Bufon, Tatjana
Title		Prirojene pomanjkljivosti komplementa
Translated title		Inherited complement deficiencies
Type		članek
Source		Med Razgl
Vol. and No.		Letnik 37, št. Suppl 5
Publication year		1998
Volume		str. 131-5
Language		slo
Abstract		The development of avious assay technologies and genetics has resulted in a number of clinical conditions in which the complement is implicated. For many countries, clinical "complementology" is entering into an exciting phase. The advances in the field of study of the complement system and its control are beginning to be applied in clinical settings. In three patients from 2 to 11 years old, hospitalised in our department, with meningococcal infections, we diagnosed complement deficiency of some components - C2, C7 and C8.
Summary		Razvoj preiskovalnih tehnik, ki merijo dejavnost in količino sestavin komplementnega sistema, in genetike je omogočil prepoznavanje različnih kliničnih dogajanj, v katera je vpleten komplement. Klinična "komplementologija" je v mnogih držazah v obdobju dinamičnega razvoja. Nova dogajanja na področju komplementnega sistema in nadzora ponovno pridobivajo mesto v klinični obravnavi bolnika. Pri treh bolnikih, starih 2 do 11 let, ki so ležali na naši kliniki zaradi meningokokne okužbe, smo ugotovili pomanjkanje določenih komponent komplementa - C2, C7 in C8.
Descriptors		COMPLEMENT COMPLEMENT PATHWAY, ALTERNATIVE COMPLEMENT PATHWAY, CLASSICAL