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Qaagi - Book of Why

Causes

Effects

1 ) genetic variantscausinghemoglobinopathies

genetic mutations that result in abnormal hemoglobin molecules that result in hemolytic anemia(passive) are caused byHemoglobinopathies

Detection of fetal mutationscausinghemoglobinopathies

mutations in the globin genes , which usually lead to functional loss or reduction of globin protein expression(passive) caused byhemoglobinopathies

mutations in the hemoglobin gene(passive) are caused byHemoglobinopathies Hemoglobinopathies

abnormal structure or synthesis of hemoglobin chains(passive) are caused byHemoglobinopathies

point mutation in globin gene that results in structural variant of hemoglobin(passive) are caused byHemoglobinopathies

mutations in the amino acid sequence resulting in structural hemoglobin ( Hb ) variants(passive) may be caused byHemoglobinopathies

abnormal structure of Hb•   characterized by low levels of normal Hb Sickle - cell anemia ( Hemoglobin S disease(passive) caused byHemoglobinopathies•

population screening and offering genetic counseling(passive) can be prevented byHemoglobinopathies

quantitative ( α- or β - thalassemia ) or qualitative ( hemoglobin variants and sickle cell disease , SCD ) defects in hemoglobin production [ 5 , 12(passive) are caused byHemoglobinopathies

deficiencies and structural abnormalities of globin chains(passive) are caused byHemoglobinopathies

Anemia indeed and of acid inheritance of in third enzyme ... whom erythrocyteresulthemoglobinopathies

the diseasescausinghemoglobinopathies

recurrent obstruction of the microcirculation classified into abnormal molecular structure of one or more by intravascular sickling(passive) can be are caused byHemoglobinopathies

defects in the genes and by anemia(passive) are caused byHemoglobinopathies

disruptions of β - globin(passive) caused byhemoglobinopathies

CRV - repairable mutations in a globin structural gene , such as sickle cell disease(passive) caused byhemoglobinopathies

the HBB genecausinghemoglobinopathies

the molecular lesionscausinghemoglobinopathies

that are worst affected with these cases in Tunisiato preventhemoglobinopathies

the key elementsto preventhemoglobinopathies

Polycythemia vera ... a rare blood diseasecauseshemoglobinopathies

Between 1.5 and 7 % of the world population ... the genescausehemoglobinopathies

all of the following structural defects(passive) can be caused byHemoglobinopathies

β chain variants that are highly unstable(passive) caused byhemoglobinopathies

6(3-fusion genes(passive) caused byhemoglobinopathies

which aimto preventhemoglobinopathies

builtto leadhemoglobinopathies

hemolytic diseases such as sickle cell anemia and thalassemiacausinghemolytic diseases such as sickle cell anemia and thalassemia

hemolytic diseases such as sickle cell anemia cllasses thalassemiacausinghemolytic diseases such as sickle cell anemia cllasses thalassemia

hemolytic diseases such as sickle cell anemia binary tradingcausinghemolytic diseases such as sickle cell anemia binary trading

microcytic anemiacausingmicrocytic anemia

binary option trading strategies youtube diseases such as sickle cell anemia and thalassemiacausingbinary option trading strategies youtube diseases such as sickle cell anemia and thalassemia

a chronic hemolytic anemia occurring almost exclusively in blackscausesa chronic hemolytic anemia occurring almost exclusively in blacks

from mutations that produce alterations in the structure of hemoglobinresultfrom mutations that produce alterations in the structure of hemoglobin

when there is altered structure , function or production of hemoglobinresultwhen there is altered structure , function or production of hemoglobin

health problemscausehealth problems

unstable hemoglobins[13causingunstable hemoglobins[13

unstable hemoglobins[19causingunstable hemoglobins[19

when there is a problem with the protein ( hemoglobin ) in the red blood cells that carry oxygen to our tissues and organsresultwhen there is a problem with the protein ( hemoglobin ) in the red blood cells that carry oxygen to our tissues and organs

to physical and chemical alterations in the function of the hemoglobin moleculeleadto physical and chemical alterations in the function of the hemoglobin molecule

a shift to the left in the Hb distributioncan causea shift to the left in the Hb distribution

disease through structural defects of hemoglobincausedisease through structural defects of hemoglobin

to decreased production of globin chains ( [ alpha ] or [ betaleadto decreased production of globin chains ( [ alpha ] or [ beta

HbA1c determination methodsinfluencingHbA1c determination methods

The Normochromic Anemias(passive) Caused byThe Normochromic Anemias

from molecular substitutions within the Hb chainresultfrom molecular substitutions within the Hb chain

in abnormal shapescan also resultin abnormal shapes

from the combination of variant alpha chains with normal or abnormal beta chainsresultingfrom the combination of variant alpha chains with normal or abnormal beta chains

from the abnormal structure or underproduction of hemoglobinresultingfrom the abnormal structure or underproduction of hemoglobin

them to ask for a genetic counselling during which they were identified as couples at risk for hemoglobinopathiesleadingthem to ask for a genetic counselling during which they were identified as couples at risk for hemoglobinopathies

in Africaso far discoveredin Africa

to reduction of RESleadto reduction of RES

the normocytic anemias(passive) caused bythe normocytic anemias

a mild ... http://www.merck.com/mrksearch/SearchServlet?filtN=professiocausesa mild ... http://www.merck.com/mrksearch/SearchServlet?filtN=professio

to a false reading on the A1c ... and which I do n't havemay leadto a false reading on the A1c ... and which I do n't have

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