Page 338 - Clinical Hematology_ Theory _ Procedures ( PDFDrive )

322 PART 4 ■ Erythrocyte Disorders

FIGURE 17.7 H S/β m . (R m A SC.

Anderson’s Atlas o Hematology, P , PA: W K

H /L W m & W k , C ,

m .)

m m m . S m

% .

P H A (S β -

m ) SS . T

S β+ m m k m m H A

x m m .

S β m x m

m m . T

m m , m - FIGURE 17.8 H SS SC. A. S k m . B. H SC -

m , , , , , k . (R m G JP, . Wintrobe’s Clinical Hematology,

. H m % % , P , PA: L W m & W k , ,

m S % % (F). T m .)

m SS . S m m

q m . m m .

H S/β m SCD. T m k m m.

m , m mm . C m mm , m

m m , m

(B x . ).
Sickle-C Disease

I H SC , H S C,

H A m H F. BOX 17.4

T m

SCD x : -

, m , Abnormalities Reported w ith Sickle Cell Trait

m m m ASSOCIATIONS WITH SICKLE CELL TRAIT VERY

. M m % LIKELY

m / L. S k S

m , x m % H

m . H m

T m . B

T m z SC (F . . )

m mm m SS , ASSOCIATION WITH SICKLE CELL TRAIT POSSIBLE

q H C % H S. T - P m m m

m SC . T C m q

SC AS ( . ., k R

) . F , SC , P

m A

H C. S , SC I k x (

% H S SA . P m m )

SC x m m m