Clinical and laboratory characteristics of patients with sickle-cell and autoimmune/connective tissue diseases

Salam Alkindi, Mustafa Al-Maini, Anil Pathare

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Patients with sickle-cell disease who develop autoimmune connective tissue disorders can present with similar clinical manifestations and/or complications making them indistinguishable. We report here a single-institution study on a cohort of 24 patients, with the above combination. The results suggest that there is often a significant delay in making the second diagnosis because of the overlapping clinical profile. It is emphasized that the clinician should be aware of and vigilant about such cases and should diligently follow up such cases to make an early diagnosis and start the appropriate treatment.

Original languageEnglish
Pages (from-to)373-378
Number of pages6
JournalRheumatology International
Volume32
Issue number2
DOIs
Publication statusPublished - Feb 2012

Fingerprint

Connective Tissue Diseases
Sickle Cell Anemia
Connective Tissue
Early Diagnosis
Therapeutics

Keywords

  • Anemia
  • Autoimmune
  • Connective
  • CTD
  • SCD
  • Sickle
  • SLE

ASJC Scopus subject areas

  • Rheumatology
  • Immunology
  • Immunology and Allergy

Cite this

Clinical and laboratory characteristics of patients with sickle-cell and autoimmune/connective tissue diseases. / Alkindi, Salam; Al-Maini, Mustafa; Pathare, Anil.

In: Rheumatology International, Vol. 32, No. 2, 02.2012, p. 373-378.

Research output: Contribution to journalArticle

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