Literature DB >> 17004533

Retinitis pigmentosa and hypogammaglobulinemia.

John C Starr1, George W Brasher, John Dominguez, Arundhati Rao.   

Abstract

This report describes a family demonstrating an unusual association of retinitis pigmentosa and hypogammaglobulinemia. The proband in this family suffered from another rare illness, ie, Sertoli cell only syndrome. The incidence of retinitis pigmentosa is 1 in 5,000 and that of common variable immunodeficiency state is 1 in 100,000, making a chance association of these illnesses very unlikely.

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Year:  2006        PMID: 17004533     DOI: 10.1097/01.smj.0000203923.89986.58

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  4 in total

1.  Metachronous Diffuse Large B-Cell Lymphoma and Kaposi Sarcoma of the Right Eyelid and Lacrimal Gland in a Patient with Granulomatous Common Variable Immunodeficiency.

Authors:  Sophie Stenton; Malee Fernando; Zanna Currie; Hardeep Singh Mudhar
Journal:  Ocul Oncol Pathol       Date:  2016-03-05

2.  AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY.

Authors:  Luke A Wiley; Elaine M Binkley; Adam P DeLuca; Grefachew Workalemahu; Nicole J Tatro; Meagan A Luse; Elizabeth L Kennedy; James C Folk; Todd E Scheetz; Zuhair K Ballas; Budd A Tucker; Robert F Mullins; Ian C Han; Edwin M Stone
Journal:  Retin Cases Brief Rep       Date:  2022-01-01

Review 3.  Ocular involvement in primary immunodeficiency diseases.

Authors:  Sima Hosseinverdi; Hassan Hashemi; Asghar Aghamohammadi; Hans D Ochs; Nima Rezaei
Journal:  J Clin Immunol       Date:  2013-11-30       Impact factor: 8.542

4.  A COVID-19 family cluster with retinitis pigmentosa and hypogammaglobulinemia.

Authors:  Abeer N Alshukairi; Yasser A Aldabbagh; Najla M Sayes; Manal M Al Gethamy; Mohammed G Alghamdi; Zuhair A Rahbeeni; Ashraf Dada
Journal:  Ann Thorac Med       Date:  2022-01-14       Impact factor: 2.219

  4 in total

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