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4,485 Possible Causes for HBS

  • Anemia

    The Hb levels did not significantly vary between pregnant and non-pregnant women.[] The admitting hematocrits (Hct) and hemoglobins (Hb) were higher in the survivors (Hct 13.6%, HB 4.7 g/dl) than in those who died (Hct 10.5%, Hb 3.8 g/dl).[] Hb can be an easily available prognostic marker for risk stratification in these patients.[]

  • Hemoglobinopathy

    Other variants include Hb Q India, Hb Lepore, Hb J Meerut, Hb D Iran, etc. These variants show heterozygous state along with beta thalassemia.[] Hemoglobin (Hb) Bristol-Alesha is caused by a GTG -- ATG mutation at codon 67 in the Hb beta chain, resulting in abnormal beta globin chains with mutated molecules from normal[] DNA sequencing analysis revealed the presence of a double heterozygous status for Hb Fontainebleau/Hb D-Punjab.[]

  • Hepatoblastoma

    HB.[] Subsequent expression analysis of primary HB and HB cell lines revealed a general overexpression of HDAC1 and HDAC2, which has been suggested to be predictive for the efficacy[] Three FAP families (2.65%) had an HB association.[]

  • Thalassemia

    KEYWORDS: Hb Constant Spring (Hb CS); Hb Quong Sze (Hb QS); compound heterotozygosity; nondeletional; α-Thalassemia (α-thal)[] By using an optimized blood lysate dilution, the HbF could be measured with no interference from hemoglobin Bart's (Hb Bart's) and hemoglobin Portland (Hb Portland 1) presented[] , hypochromia and a normal Hb A2 level.[]

  • Hemoglobin Bart's Disease

    Fetal blood samples were collected for fetal Hb typing and hemoglobin (Hb) levels.[] Hb Bart's predictive model included AFP and uE3 is relatively effective and may be helpful in Hb Bart's prenatal screening.[] PlGF, sFlt-1, and sFlt-1/PlGF ratio were compared between the fetal Hb Bart's group and the non-Hb Bart's group (normal Hb typing or α-thalassemia-1 carrier).[]

  • Alpha Thalassemia

    The other is the first reported case of compound heterozygosity for Hb S and an unstable hemoglobin, Hb Volga.[] Family studies identified that her father and sister were double heterozygotes for Hb Korle-Bu and alpha-thal-1, whereas her mother was a double heterozygote for Hb E/Hb Constant[] Hb Bart's hydrops fetalis is a lethal form in which no α-globin chain is synthesized.[]

  • Iron Deficiency

    […] patients with Hb 13 g/dl.[] Hemoglobin (Hb) was determined by a portable photometer (Hemocue Hb201 ), and anemia was defined as altitude-adjusted Hb 110 g/L.[] Child was put on steroids and despite severe anaemia (Hb 3.2 g/dl), he showed improvement and survived.[]

  • Hemoglobin SC Disease

    […] of Hb C and Hb A to copolymerize with Hb S.[] Hb SC, and one Hb CC.[] In HbSC disease red cells contain equal levels of HbS and HbC.[]

  • Sickle Cell Disease

    Hb F levels after HU therapy positively correlated with the duration of HU therapy, baseline Hb F levels and baseline total hemoglobin (Hb) (r   0.4, p   0.04; r   0.45, p[] SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis (disorder) Sickle-cell/Hb-C disease without crisis hemoglobin SC disease Sickle-cell[] We aimed to evaluate the long-term effects of HU therapy on Hb F and assess its long term efficacy and safety in sickle cell disease patients.[]

  • Thalassemia Minor

    However, there is less evidence for β-thal minor and Hb H (β4) disease on its association with oxidation status.[] Abstract The Lepore hemoglobins (Hbs) are a group of structural defects resulting from different recombination events between the delta- and beta-globin genes.[] […] as Hb Constant Spring, Hb Paksé, Hb Quong Sze, and Hb Pak Num Po.[]

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