Bloom Syndrome: Presentation of Two Siblings


  • Safa Barış
  • Elif Karakoç Aydıner
  • Ahmet Özen
  • Cevdet Özdemir
  • Nerin N. Bahçeciler
  • Işıl B. Barlan


Bloom syndrome, pediatrics, immunodeficiency


Bloom syndrome is a rare autosomal recessive syndrome characterized by proportional dwarfism, characteristic facial findings, photosensitivity, telangiectasia, well-circumscribed dermal hypo- or hyperpigmented lesions, immunodeficiency, and infertility. Ten- and 3-year-old sibling patients were thought to have Bloom syndrome due to failure to thrive, café-au-lait spots and giant nevi on the legs. The older sibling was operated for Wilms’ tumor at 4 years of age. The diagnosis was confirmed with increased sister chromatid exchanges in peripheral blood cells in both cases. In patients with Bloom syndrome, prevention of recurrent respiratory and gastrointestinal infections and close monitoring of the patients regarding immunodeficiency and endocrinologic diseases are important issues. In Bloom syndrome, the mutation in the 15q26.1 region of the BLM gene, leading to protein loss and increased frequency of sister chromatid exchanges, promotes malignancy formation. Minimization of sun exposure is important in terms of malignancy development, which is the main cause of deaths in the 2nd and 3rd decades. In this report, we aimed to present information about the clinical findings, prognosis and immunological features of Bloom syndrome.


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How to Cite

Barış S, Karakoç Aydıner E, Özen A, Özdemir C, Bahçeciler NN, Barlan IB. Bloom Syndrome: Presentation of Two Siblings. AAI [Internet]. 2010 May 15 [cited 2022 Jan. 24];8(1):64-8. Available from:



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