CLASIFICAREA FREDRICKSON Flashcards

1
Q

TIPUL 1

A

cresc chilomicronii
scaderea lipoproteinlipazei ( hidrolizeaza TG din chilomicroni), alterarea ApoC2

Sindr Buerger - Gruetz
Hiperlipoproteinemia familiala
Hiperchilomicronemia familiala

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2
Q

tipul IIa

A

crestere LDL
Hipercoloesterolemia poligenica
Hipercolesterolemia familiala

deficit de receptori LDL

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3
Q

tipul II B

A

cresc LDL si VLDL
scad receptorii pt LDL si cresre ApoB
Hiperlipidemie combinata

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4
Q

tipul III

A

creste IDL
Disbetalipoproteinemia familiala
pert cat IDL prin apo E2 anormala si deficit de lipaza hepatica

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5
Q

tipul iv

A

creste VLDL
Hiperlipemia endogena
productie de VLDL si scaderea eliminarii

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6
Q

tipul V

A

Hipertrigliceridemie familiala
Crestere VLDL si chiliomicroni

apo C3 anormala (C32) scaderea reaportului apo C2/ Apoc3 sinteza de apo E4 anormala

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7
Q

HIPERCOLESTEROLEMIE FAMILIALA

A

tip IIa
creste LDL
defect al receptorului LDL —> scadere a clearenceului LDL cu o crestere a sintezei de LDL
acumulare intracel –> xantoame, xantelasma
acumularee xtracel –>ateroscleroza

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8
Q

DEFICIT FAMILIAL DE APO B 100

A

imposibilitate recunoasterii LDL de catre repectorii specifici
acumulare de LDL
cons asemenea hipercoloesterolemiei familiale

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9
Q

hipercolesterolemia comuna

A

creste sinteza LDL
scade catabolismul
risc de ateroscleroza dar FARA XANTOAME

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10
Q

Deficit familial de LPL

A

LPL- lipoproteinlipaza
impos de metab a chilomicronilor
lipaza pabncreatica ii trans in compusi toxici –> pancreatita (copil - dureri abd acute)
chilomicr in macrofage –> hepato-splenomegalie
cel spumoasa in mad osoasa
opacitati corneene
xantoame

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11
Q

hipertrigliceridemia familiala

A

sint crescuta de Tg si VLDL
catabolism VLDL scazut
risc de cardiopatie ischemica

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12
Q

deficit familial de aop C2

A

insuf functionala a LPL
cu acumulare de chilomicroni si VLDL
sindrom clinic asemanator cu def de LPL

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13
Q

Hiperlipoproteinemie familiala combinata

A

exces de VLDL si LDL
risc crescut de ateroscleroza
nu au xantoame

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14
Q

disbetalipoproteinemia familiala

A

defect al apo E
scaderea preluarii hepatice a resturilor de chilomicroni si IDL
creste riscul ateorsclerotic si apar depuneri de colesterol (xantoame, strii palmare)

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