Genetically caused and rare forms of dyslipoproteinemias

Lipovetslkiĭ, B.M.; Trofanov, V.F.

Klinicheskaia Meditsina 62(11): 102-108

1984


ISSN/ISBN: 0023-2149
PMID: 6521363
Document Number: 229026
Subjects (40) from 15 families whose members had a history of genetically determined dyslipoproteinemia were examined. Case histories were described which included patients with homozygous type IIA DLP and types I and V DLP as well as abdominal colic syndrome and 1 female patient with Hand-Schueller-Christian disease. Out of 27 patients under observation with IIa and IIb types DLP (including 2 children under 16) coronary heart disease was found in 16 patients. Examples of the effective therapy of hyperlipidemia are given although hereditary DLP is resistant to treatment.

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