Isolated growth hormone deficiency in a patient with immunoglobulin class switch recombination deficiency

Journal of Investigational Allergology and Clinical Immunology

Volumn 19, Issue 3, 2009, Pages 233-236

  Kashef, Sara ^a   Mehdi Ghaedian, M ^b   Rezaei, N ^c,d   Karamizadeh, Z ^c   Aghamohammadi, A ^c   Durandy, A ^e   Pan Hammarstrom, Q ^f   Hammarstrom, L ^f  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Class switch recombination; Growth hormone deficiency; Hyper IgM syndrome

Indexed keywords

ANTIBIOTIC AGENT; GROWTH HORMONE; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M;

ADULT; ANAMNESIS; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CLINICAL FEATURE; DIARRHEA; GENE REARRANGEMENT; GROWTH HORMONE DEFICIENCY; HUMAN; HUMAN TISSUE; HYPER IGM SYNDROME; LABORATORY TEST; MALE; RECURRENT DISEASE; RESPIRATORY TRACT INFECTION; THORAX RADIOGRAPHY;

GROWTH HORMONE; HUMANS; HYPER-IGM IMMUNODEFICIENCY SYNDROME; IMMUNOGLOBULIN A; IMMUNOGLOBULIN CLASS SWITCHING; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; MALE; PEDIGREE; YOUNG ADULT;

EID: 67651173344     PISSN: 10189068     EISSN: 16980808     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Etzioni A, Ochs HD. The Hyper IgM Syndrome-an Evolving Story. Pediatr Res. 2004;56:519-525 (Pubitemid 39280902)
2. Geha RS, Notarangelo LD, Casanova JL, Chapel H, Conley ME, Fischer A, Hammarström L, Nonoyama S, Ochs HD, Puck JM, Roifman C, Seger R, Wedgwood J; International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. J Allergy Clin Immunol. 2007;120:776-794
3. Rezaei N, Aghamohammadi A, Moin M, Pourpak Z, Movahedi M, Gharagozlou M, Atarod L, Ghazi BM, Isaeian A, Mahmoudi M, Abolmaali K, Mansouri D, Arshi S, Tarash NJ, Sherkat R, Akbari H, Amin R, Alborzi A, Kashef S, Farid R, Mohammadzadeh I, Shabestari MS, Nabavi M, Farhoudi A. Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry. J Clin Immunol. 2006;26:519-532 (Pubitemid 44764262)
4. Durandy A, Revy P, Fischer A. Human models of inherited immunoglobulin class switch recombination and somatic hypermutation defects (hyper-IgM syndromes). Adv Immunol. 2004;82:295-330. (Pubitemid 38209514)
5. Imai K, Catalan N, Plebani A, Marodi L, Sanal O, Kumaki S, Nagendran V, Wood P, Glastre C, Sarrot-Reynauld F, Hermine O, Forveille M, Revy P, Fischer A, Durandy A. Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination. J Clin Invest. 2003;112:136-142 (Pubitemid 38056385)
6. Levy J, Espanol-Boren T, Thomas C, Fischer A, Tovo P, Bordigoni P, Resnick I, Fasth A, Baer M, Gomez L, Sanders EA, Tabone MD, Plantaz D, Etzioni A, Monafo V, Abinun M, Hammarstrom L, Abrahamsen T, Jones A, Finn A, Klemola T, DeVries E, Sanal O, Peitsch MC, Notarangelo LD. Clinical spectrum of X-linked hyper-IgM syndrome. J Pediatr. 1997;131:47-54. (Pubitemid 27498308)
7. Ming JE, Stiehm ER. Syndromic immunodeficiencies. In: Rezaei N, Aghamohammadi A, Notarangelo LD (eds). Primary immunodeficiency diseases: definition, diagnosis and management. Berlin Heidelberg, Springer-Verlag, 2008, vol 1, pp 291-314.
8. Ohzeki T, Hanaki K, Motozumi H, Ohtahara H, Hayashibara H, Harada Y, Okamoto M, Shiraki K, Tsuji Y, Emura H. Immunodeficiency with increased immunoglobulin M associated with growth hormone insufficiency. Acta Paediatr. 1993;82:620-623 (Pubitemid 23188670)
9. Moschese V, Lintzman J, Callea F, Chini L, Devito R, Carsetti R, Di Cesare S, Geissman F, Brousse N, Rossi P, Durandy A. A novel form of non-X-linked hyperigm associated with growth and pubertal disturbances and with lymphoma development. J Pediatr. 2006;148:404-406
10. Péron S, Pan-Hammarström Q, Imai K, Du L, Taubenheim N, Sanal O, Marodi L, Bergelin-Besançon A, Benkerrou M, de Villartay JP, Fischer A, Revy P, Durandy A. A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair. J Exp Med. 2007;204:1207-1216 (Pubitemid 46798162)
11. Durandy A, Peron S, Fischer A. Hyper-IgM syndromes. Curr Opin Rheumatol. 2006;18:369-376
12. Aghamohammadi A, Lougaris V, Plebani A, Miyawaki T, Durandy A, Hammarström L. Predominantly antibody deficiencies. In: Rezaei N, Aghamohammadi A, Notarangelo LD (eds). Primary immunodeficiency diseases: definition, diagnosis and management. Berlin Heidelberg, Springer-Verlag, 2008, vol 1, pp 97-130.
13. Pan-Hammarström Q, Zhao Y, Hammarström L. Class switch recombination: a comparison between mouse and human. Adv Immunol. 2007;93:1-61. (Pubitemid 46441428)