Literature DB >> 21748095

Omenn's Syndrome: A rare primary immunodeficiency disorder.

Ibtisam B Elnour1, Shakeel Ahmed, Kamal Halim, V Nirmala.   

Abstract

Over the last 17 years different forms of severe combined immunodeficiency have been diagnosed at Sultan Qaboos University Hospital, Muscat. Omenn's syndrome is a rare autosomal recessive form of severe combined immunodeficiency. We report a 6 weeks old Omani infant who presented with the characteristic clinical and immunological phenotype of Omenn's syndrome. We take the opportunity to discuss and review the immunological aspect of this rare syndrome.

Entities:  

Keywords:  Case report; Immunodeficiency, primary; Immunodeficiency, severe, combined; Oman; Omenn’s Syndrome

Year:  2007        PMID: 21748095      PMCID: PMC3074865     

Source DB:  PubMed          Journal:  Sultan Qaboos Univ Med J        ISSN: 2075-051X


  20 in total

1.  Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

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Journal:  J Clin Invest       Date:  1991-04       Impact factor: 14.808

2.  Clinical and immune recovery from Omenn syndrome after bone marrow transplantation.

Authors:  A K Junker; K W Chan; B G Massing
Journal:  J Pediatr       Date:  1989-04       Impact factor: 4.406

3.  Clinical and immunological findings in four infants with Omenn's syndrome: a form of severe combined immunodeficiency with phenotypically normal T cells, elevated IgE, and eosinophilia.

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Journal:  Clin Immunol Immunopathol       Date:  1987-08

4.  Combined immunodeficiency presenting as the Letterer-Siwe syndrome.

Authors:  S D Cederbaum; G Niwayama; E R Stiehm; R C Neerhout; A J Ammann; W Berman
Journal:  J Pediatr       Date:  1974-10       Impact factor: 4.406

5.  The lymph node pathology of Omenn's syndrome.

Authors:  J V Martin; P B Willoughby; V Giusti; G Price; L Cerezo
Journal:  Am J Surg Pathol       Date:  1995-09       Impact factor: 6.394

6.  Successful unrelated umbilical cord blood transplantation in a child with Omenn's syndrome.

Authors:  A Benito; M A Diaz; F Alonso; G Fontán; L Madero
Journal:  Pediatr Hematol Oncol       Date:  1999 Jul-Aug       Impact factor: 1.969

7.  RAG mutations in human B cell-negative SCID.

Authors:  K Schwarz; G H Gauss; L Ludwig; U Pannicke; Z Li; D Lindner; W Friedrich; R A Seger; T E Hansen-Hagge; S Desiderio; M R Lieber; C R Bartram
Journal:  Science       Date:  1996-10-04       Impact factor: 47.728

Review 8.  Omenn syndrome: a disorder of Rag1 and Rag2 genes.

Authors:  A Villa; S Santagata; F Bozzi; L Imberti; L D Notarangelo
Journal:  J Clin Immunol       Date:  1999-03       Impact factor: 8.317

9.  Omenn syndrome in an infant with IL7RA gene mutation.

Authors:  Silvia Giliani; Carmen Bonfim; Genevieve de Saint Basile; Gaetana Lanzi; Nicole Brousse; Adriana Koliski; Mariester Malvezzi; Alain Fischer; Luigi D Notarangelo; Francoise Le Deist
Journal:  J Pediatr       Date:  2006-02       Impact factor: 4.406

10.  Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome.

Authors:  S Signorini; L Imberti; S Pirovano; A Villa; F Facchetti; M Ungari; F Bozzi; A Albertini; A G Ugazio; P Vezzoni; L D Notarangelo
Journal:  Blood       Date:  1999-11-15       Impact factor: 22.113

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  6 in total

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Authors:  Aurora Irene Idilli; Francesca Precazzini; Maria Caterina Mione; Viviana Anelli
Journal:  Genes (Basel)       Date:  2017-09-20       Impact factor: 4.096

2.  The R229Q mutation of Rag2 does not characterize severe immunodeficiency in mice.

Authors:  Young Jin; Ara Lee; Ja Hyun Oh; Han-Woong Lee; Sang-Jun Ha
Journal:  Sci Rep       Date:  2019-03-14       Impact factor: 4.379

3.  An infant with omenn syndrome: A case report.

Authors:  Ubaid Khan; Rana Uzair Ahmad; Ayesha Aslam
Journal:  Ann Med Surg (Lond)       Date:  2022-01-28

4.  Case Report: "Primary Immunodeficiency"-Severe Autoimmune Enteropathy in a Pediatric Heart Transplant Recipient Treated With Abatacept and Alemtuzumab.

Authors:  Elizaveta Kalaidina; Elizabeth C Utterson; Deepa Mokshagundam; Mai He; Shalini Shenoy; Megan A Cooper
Journal:  Front Immunol       Date:  2022-04-05       Impact factor: 8.786

5.  The value of family history in diagnosing primary immunodeficiency disorders.

Authors:  Mohamed A Hendaus; Ahmad Alhammadi; Mehdi M Adeli; Fawzia Al-Yafei
Journal:  Case Rep Pediatr       Date:  2014-08-05

6.  CD3ε+ Cells in Pigs With Severe Combined Immunodeficiency Due to Defects in ARTEMIS.

Authors:  Adeline N Boettcher; A Giselle Cino-Ozuna; Yash Solanki; Jayne E Wiarda; Ellie Putz; Jeana L Owens; Sara A Crane; Amanda P Ahrens; Crystal L Loving; Joan E Cunnick; Raymond R R Rowland; Sara E Charley; Jack C M Dekkers; Christopher K Tuggle
Journal:  Front Immunol       Date:  2020-03-31       Impact factor: 7.561

  6 in total

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