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An investigation of muscle strength, endurance and quality of life in South African children with haemophilia: a pilot studyFaris, DonnaTeresa 10 November 2011 (has links)
Haemophilia is an X-linked genetically transmitted disorder that is characterised by a
deficiency in a circulating blood clotting factor (Falk et al 2000) and presents with intraarticular
and intramuscular bleeding. Haemophilia A is the most common and results from a
deficiency of clotting factor VIII (Barlow et al 2007). Haemophilia B results from a
deficiency of clotting factor IX. Haemophilia A and B are described as having an incidence of
approximately 1:10 000 and 1:60 000 people respectively (Engelbert et al 2007). Both
haemophilia A and B are rare disorders, but are the most common, severe inherited bleeding
disorder (Price et al 2007).
The haemostatic defects of haemophilia lead to spontaneous and post-traumatic internal
bleeding events (Von Mackensen et al 2004). Hilberg et al (2001) and Ghosh et al (2004)
reported on the consequences of repeated bleeds and immobilization resulting in muscle
atrophy, chronic synovitis, chronic haemophilic arthropathy, contractures, unequal leg lengths
and loss of proprioception. Considering the musculoskeletal implications of haemophilia,
Bradley et al (2006) reported that haemophilia may have a significant impact on the quality of
life (QoL). Varni et al (2006) stated that children with chronic health conditions were reported
to not only experience lower physical functioning, but also manifested lower emotional, social
and school functioning in comparison with healthy children.
The main aim of this study is to compare the muscle strength, endurance and QoL of a group
of children with haemophilia to a group of aged matched healthy peers. Children between the
ages of five and sixteen years were included in the study.
The MicroFET 2 dynamometer has been used to assess the muscle strength of each subject
and the Six Minute Walk Test has been used to test submaximal endurance levels of each
group. The PedsQL is one of the quality of life assessment tools used to compare both groups,
where the HAEMO-QOL has been used specifically to test the subjects with haemophilia. The
first group of participants consisted of children having a diagnosis of haemophilia (n=15), and
the second comparative group consisted of normally developing children (n=18).
The results were analysed and compared using the student t-test and the Pearson’s correlation
coefficient. The two groups were well matched for all anthropometric data. With regards to
muscle strength, the haemophilia group showed significant weakness with regards to their left (L) elbow extensors and right (R) knee extensors in comparison to control group, with p
values as p <0.01 and p< 0.05 respectively. In contrast the haemophiliac group showed
significantly greater strength in the (L) and (R) ankle dorsiflexors, in comparison to the
control group with p values as p<0.02 and p<0.00 respectively. No statistical significance was
demonstrated in the 6MWT and QoL measures used between the two groups.
The children with haemophilia in comparison to a healthy sample of age matched peers
demonstrated almost equal abilities in measured muscle strength and submaximal endurance
levels, and almost equal scores in the PedsQL of 75.5% and 77.7 % questionnaire indicating
high perceived quality of life in both groups. There was a positive correlation between the
Haemo-QoL questionnaire and the PedsQL questionnaire in the haemophilia group,
indicating, again, high perceived quality of life with no discrepancies between the two
questionnaires used.
The findings of this study demonstrate a need for further research on haemophilic subjects in
a South African context. However, the results have shown that both the groups in this present
study have reduced muscle strength and poor endurance in comparison to international trends.
With regards to perceived QoL, the boys with haemophilia had scores which were similar to
those obtained in other studies.
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Hemofilia e estados hemofiliódes no Rio Grande do Sul freqüência, fisiologia e herana̧ /Roisenberg, Israel. January 1971 (has links)
Thesis--Universidade Federal do Rio Grande do Sul. / Includes bibliographical references (p. 119-124).
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Haemophilic diseases in Denmark; a classification of the clotting defects in 78 haemophilic families. [Tr. from the DanishSjølin, Knud Erik. January 1960 (has links)
Afhandling - Copenhagen, 1959. / Summary in Danish.
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Hemofilia e estados hemofiliódes no Rio Grande do Sul freqüência, fisiologia e herana̧ /Roisenberg, Israel. January 1971 (has links)
Thesis--Universidade Federal do Rio Grande do Sul. / Includes bibliographical references (p. 119-124).
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Haemophilic diseases in Denmark; a classification of the clotting defects in 78 haemophilic families. [Tr. from the DanishSjølin, Knud Erik. January 1960 (has links)
Afhandling - Copenhagen, 1959. / Summary in Danish.
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Pharmacokinetic dosing of factor VIII and factor IX in prophylactic treatment of haemophiliaCarlsson, Maj. January 1997 (has links)
Thesis (doctoral)--Lund University, 1997. / Added t.p. with thesis statement inserted.
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Pharmacokinetic dosing of factor VIII and factor IX in prophylactic treatment of haemophiliaCarlsson, Maj. January 1997 (has links)
Thesis (doctoral)--Lund University, 1997. / Added t.p. with thesis statement inserted.
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An investigation of psychosocial attributes in adult males with hemophilia a thesis submitted in partial fulfillment ... /Walsh, Kathleen Kelley. January 1988 (has links)
Thesis (M.S.)--University of Michigan, 1988.
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An investigation of psychosocial attributes in adult males with hemophilia a thesis submitted in partial fulfillment ... /Walsh, Kathleen Kelley. January 1988 (has links)
Thesis (M.S.)--University of Michigan, 1988.
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The molecular basis of hemophilia B : identification of the defect in factor IXVancouverGeddes, Valerie Anne January 1987 (has links)
Hemophilia BVancouver, is a moderately severe hereditary disorder in which the factor IX antigen is present in relatively normal amounts but the biological activity of factor IX is markedly reduced. Previous studies have demonstrated that although the patient has 62% of the normal factor IX antigen level in his plasma, he shows only 2.6% of normal factor IX procoagulant activity. In addition, radioimmunoassays have shown that epitopes on both the heavy and light chains of activated factor IX are present. These two results were taken as an indication that the molecular defect causing the hemophilia may be a point mutation involving an amino acid change in the protein. In order to identify the mutation involved, DNA was isolated from lymphocytes in a blood sample from the patient. This DNA was used to construct a genomic library in the λ vector EMBL3. One million of the resultant clones were screened with a labelled factor IX cDNA probe to identify those clones containing portions of the factor IX
gene. DNA inserts from three λ clones, which together span the entire gene, were subcloned to facilitate sequence analysis of the exons and intron / exon junctions of the factor IX gene. The nucleotide sequences of the coding regions were found to match the published sequence of the normal gene, except for one nucleotide. A single mutation was found at nucleotide 31,311 of the factor IX gene (Yoshitake et al.,1985), corresponding to amino acid 397 of the mature protein. This alteration, which changes an isoleucine codon, ATA, to a threonine codon, ACA, is novel among the mutations which have been reported to cause hemophilia B. A three dimensional model of the protease domain of factor IXа, which was prepared on the basis of its homology to the pancreatic serine proteases, was examined in the vicinity of residue 397. The position of threonine 397 in this model suggests that this mutation could alter the hydrogen bonding between factor IXа and its substrate, factor X. Taken together, these data suggest that this mutation is the cause of the hemophilia in this patient. / Medicine, Faculty of / Medical Genetics, Department of / Graduate
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