Page last updated: 2024-10-25

deferoxamine and Stunted Growth

deferoxamine has been researched along with Stunted Growth in 25 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Research Excerpts

ExcerptRelevanceReference
" The severe toxic effects on vision, hearing and growth are all more likely at higher doses of DF and there appears to be partial protection against them by iron overload."2.38The toxic effects of desferrioxamine. ( Huehns, ER; Porter, JB, 1989)
"Hypogonadism was noted in 59% of the patients who reached pubertal age, and short stature was found in 36% of patients who reached final height."1.33Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients. ( Carmi, D; Kornreich, L; Miskin, H; Phillip, M; Shalitin, S; Tamary, H; Weintrob, N; Yaniv, I; Zilber, R, 2005)
"Dental caries were significantly higher in thalassemics."1.33Physical growth patterns and dental caries in thalassemia. ( Dewan, P; Gomber, S, 2006)
"A male thalassemia major patient who developed bone and cartilage abnormalities with a standard dose of desferrioxamine (DFX) given subcutaneously from the age of 4 years was treated with the oral iron chelator deferiprone (L1)."1.31Treatment with deferiprone (L1) in a thalassemic patient with bone lesions due to desferrioxamine. ( Campisi, S; De Sanctis, V; Di Silvestro, G; Mangiagli, A; Urso, L, 2000)
"Since patients with thalassemia are not growth hormone deficient, the data suggest the possibility of defective hepatic biosynthesis of somatomedin."1.26Depressed serum somatomedin activity in beta-thalassemia. ( Graziano, JH; Hilgartner, MW; Levine, LS; Markenson, AL; New, MI; Saenger, P; Schwartz, E, 1980)

Research

Studies (25)

TimeframeStudies, this research(%)All Research%
pre-199012 (48.00)18.7374
1990's8 (32.00)18.2507
2000's5 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Shalitin, S1
Carmi, D1
Weintrob, N1
Phillip, M1
Miskin, H1
Kornreich, L1
Zilber, R1
Yaniv, I1
Tamary, H1
Gomber, S1
Dewan, P1
Pomarède, R1
Girot, R1
Constant, S1
Rappaport, R1
Ley, TJ1
Griffith, P1
Nienhuis, AW1
Saenger, P1
Schwartz, E1
Markenson, AL1
Graziano, JH1
Levine, LS1
New, MI1
Hilgartner, MW1
Borgna-Pignatti, C2
Zurlo, MG1
DeStefano, P1
Boffa, C1
DeSanctis, V1
DiPalma, A1
DiGregorio, L1
Melevendi, C2
Piga, A2
Sabato, V1
Giardina, PJ1
Grady, RW1
Albo, C1
Cabrera, J1
Dios, A1
Castro, M1
Ares, C1
Constenla, I1
López, D1
Naselli, A2
Vignolo, M1
Di Battista, E1
Garzia, P1
Forni, GL1
Traverso, T1
Aicardi, G1
Cavallo, L1
Gurrado, R1
Zecchino, C1
Manolo, F1
De Sanctis, V3
Cisternino, M1
Caruso-Nicoletti, M2
Galati, M1
Di Bella, D1
Pizzarelli, G1
Leonardi, C1
Sciuto, C1
Coco, M1
Di Gregorio, F1
Mangiagli, A1
Campisi, S1
Di Silvestro, G1
Urso, L1
Taher, A1
Sheikh-Taha, M1
Koussa, S1
Inati, A1
Neeman, R1
Mourad, F1
Viprakasit, V1
Tanphaichitr, VS1
Mahasandana, C1
Assteerawatt, A1
Suwantol, L1
Veerakul, G1
Kankirawatana, S1
Pung-Amritt, P1
Suvatte, V1
Cividalli, G1
O'Brien, RT2
Pearson, HA1
Orzincolo, C1
Scutellari, PN1
Castaldi, G1
Davies, SC1
Wonke, B1
Porter, JB1
Huehns, ER1
De Virgiliis, S1
Congia, M1
Frau, F1
Argiolu, F1
Diana, G1
Cucca, F1
Varsi, A1
Sanna, G1
Podda, G1
Fodde, M1
Luzzatto, L1
Capalbo, P1
Gambotto, S1
Tricta, F1
Gabutti, V2
Festa, RS1
De Stefano, P1
Zonta, L1
Vullo, C1
Masera, G1
Terzoli, S1
Wolman, IJ1
Ortolani, M1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Safety & Efficacy of Thalidomide in Children With Transfusion Dependent Thalassemia: a Quasi Randomized Control Trial in a Tertiary Care Hospital in Bangladesh[NCT06098014]Phase 360 participants (Anticipated)Interventional2023-03-08Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

6 reviews available for deferoxamine and Stunted Growth

ArticleYear
Transfusion haemosiderosis and chelation therapy.
    Clinics in haematology, 1982, Volume: 11, Issue:2

    Topics: Adolescent; Adult; Ascorbic Acid; Blood Transfusion; Cardiomyopathies; Deferoxamine; Dose-Response R

1982
Chelation therapy in beta-thalassemia: the benefits and limitations of desferrioxamine.
    Seminars in hematology, 1995, Volume: 32, Issue:4

    Topics: Adolescent; Adult; Chelating Agents; Chelation Therapy; Child; Deferoxamine; Growth Disorders; Heari

1995
Iron overload: clinical and pathologic aspects in pediatrics.
    Seminars in hematology, 1977, Volume: 14, Issue:1

    Topics: Abnormalities, Multiple; Adolescent; Adult; Ascorbic Acid Deficiency; Bloodletting; Child; Child, Pr

1977
The management of haemoglobinopathies.
    Bailliere's clinical haematology, 1991, Volume: 4, Issue:2

    Topics: Adolescent; Anemia, Sickle Cell; Bone Marrow Transplantation; Chelation Therapy; Child; Child, Presc

1991
The toxic effects of desferrioxamine.
    Bailliere's clinical haematology, 1989, Volume: 2, Issue:2

    Topics: Animals; Blood-Brain Barrier; Deferoxamine; Disease Susceptibility; Eye Diseases; Growth Disorders;

1989
Modern management of thalassemia.
    Pediatric annals, 1985, Volume: 14, Issue:9

    Topics: Adolescent; Arrhythmias, Cardiac; Ascorbic Acid; Blood Transfusion; Child; Cholelithiasis; Deferoxam

1985

Trials

1 trial available for deferoxamine and Stunted Growth

ArticleYear
Comparison between deferoxamine and deferiprone (L1) in iron-loaded thalassemia patients.
    European journal of haematology, 2001, Volume: 67, Issue:1

    Topics: Administration, Oral; Adolescent; Adult; beta-Thalassemia; Chelation Therapy; Child; Deferiprone; De

2001

Other Studies

18 other studies available for deferoxamine and Stunted Growth

ArticleYear
Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients.
    European journal of haematology, 2005, Volume: 74, Issue:2

    Topics: Adolescent; Adult; beta-Thalassemia; Biomarkers; Body Height; Child; Child, Preschool; Deferoxamine;

2005
Physical growth patterns and dental caries in thalassemia.
    Indian pediatrics, 2006, Volume: 43, Issue:12

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferiprone; Deferoxamine; Dental Caries; Female; Ferrit

2006
[Effect of hematologic treatment on the growth and puberty of children with thalassemia major].
    Archives francaises de pediatrie, 1984, Volume: 41, Issue:4

    Topics: Adolescent; Blood Transfusion; Body Height; Child; Combined Modality Therapy; Deferoxamine; Female;

1984
Depressed serum somatomedin activity in beta-thalassemia.
    The Journal of pediatrics, 1980, Volume: 96, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Female; Growth Disorders; Hemosiderosis; H

1980
Outcome of thalassemia treated with conventional therapy.
    Bone marrow transplantation, 1993, Volume: 12 Suppl 1

    Topics: Adolescent; beta-Thalassemia; Blood Transfusion; Cardiovascular Diseases; Cause of Death; Chelation

1993
[Program of hypertransfusion and chelation with desferrioxamine in 10 patients with thalassemia major].
    Sangre, 1995, Volume: 40, Issue:6

    Topics: Adolescent; beta-Thalassemia; Blood Transfusion; Chelation Therapy; Child; Combined Modality Therapy

1995
Long-term follow-up of skeletal dysplasia in thalassaemia major.
    Journal of pediatric endocrinology & metabolism : JPEM, 1998, Volume: 11 Suppl 3

    Topics: Adolescent; Adult; beta-Thalassemia; Blood Transfusion; Body Height; Bone Diseases, Developmental; D

1998
Short-term therapy with recombinant growth hormone in polytransfused thalassaemia major patients with growth deficiency.
    Journal of pediatric endocrinology & metabolism : JPEM, 1998, Volume: 11 Suppl 3

    Topics: Adolescent; Age Determination by Skeleton; beta-Thalassemia; Blood Transfusion; Body Height; Child;

1998
Growth failure and bone lesions due to desferrioxamine in thalassaemic patients.
    Journal of pediatric endocrinology & metabolism : JPEM, 1998, Volume: 11 Suppl 3

    Topics: beta-Thalassemia; Blood Transfusion; Bone Diseases; Chelating Agents; Child; Deferoxamine; Female; G

1998
Treatment with deferiprone (L1) in a thalassemic patient with bone lesions due to desferrioxamine.
    Journal of pediatric endocrinology & metabolism : JPEM, 2000, Volume: 13, Issue:6

    Topics: beta-Thalassemia; Body Height; Bone Diseases; Deferiprone; Deferoxamine; Growth Disorders; Humans; I

2000
Linear growth in homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients under different treatment regimens.
    Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 2001, Volume: 84, Issue:7

    Topics: beta-Thalassemia; Blood Transfusion; Body Height; Body Weight; Chi-Square Distribution; Child; Defer

2001
The clinical management of homozygous beta-thalassemia.
    Haematologica, 1979, Volume: 64, Issue:1

    Topics: Blood Transfusion; Deferoxamine; Endocrine System Diseases; Growth Disorders; Humans; Splenectomy; T

1979
The management of thalassemia major.
    Seminars in hematology, 1975, Volume: 12, Issue:3

    Topics: Adolescent; Adult; Blood Transfusion; Chelating Agents; Child; Child, Preschool; Deferoxamine; Diet

1975
Growth plate injury of the long bones in treated beta-thalassemia.
    Skeletal radiology, 1992, Volume: 21, Issue:1

    Topics: Adolescent; Chelation Therapy; Child; Child, Preschool; Deferoxamine; Female; Follow-Up Studies; Gro

1992
Deferoxamine-induced growth retardation in patients with thalassemia major.
    The Journal of pediatrics, 1988, Volume: 113, Issue:4

    Topics: Body Height; Bone and Bones; Deferoxamine; Dose-Response Relationship, Drug; Female; Growth Disorder

1988
High-dose desferrioxamine as a cause of growth failure in thalassemic patients.
    European journal of haematology, 1988, Volume: 40, Issue:4

    Topics: Child; Child, Preschool; Deferoxamine; Female; Ferritins; Growth Disorders; Humans; Male; Thalassemi

1988
Growth and sexual maturation in thalassemia major.
    The Journal of pediatrics, 1985, Volume: 106, Issue:1

    Topics: Adolescent; Adult; Age Determination by Skeleton; Amenorrhea; Blood Transfusion; Body Height; Child;

1985
Some clinical features of Cooley's anemia patients as related to transfusion schedules.
    Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1

    Topics: Blood Transfusion; Deferoxamine; Fetal Hemoglobin; Growth Disorders; Hematopoiesis; Humans; Iron; Li

1969