Abstract
Introduction: Bloom syndrome is a rare autosomal recessive disorder characterized by chromosomal instability caused by mutations in the BLM gene that increase the risk of developing neoplasia, particularly at an early age. Bloom syndrome is typically characterized by short stature, photosensitivity, telangiectatic erythema, learning difficulties, immunodeficiency, and malignancy. Case report: We report a case of an adolescent girl with short stature and recurrent infections, who does not present typical erythematous sun-sensitive skin lesions to the face and whose high-pitched voice led to the diagnosis of BS caused by a novel L753X mutation. Discussion: To date, she has not presented with any malignancy or characteristic malar rash.
Original language | English |
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Pages (from-to) | 193-198 |
Number of pages | 6 |
Journal | Portuguese Journal of Pediatrics |
Volume | 55 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1 Jul 2024 |
Keywords
- Bloom syndrome
- Case report
- Chromosomal instability
- Novel mutation
- Sister chromatid exchange