This case report presents the first H-syndrome rarity in Iraq, a 12-year-old female patient who was attending the Rheumatology out clinic for progressive hands joint deformities. She has a history of a multi-systemic collection of diseases with various clinical features that include beta thalassemia minor, sensorineural deafness, and celiac disease.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761660 | PMC |
http://dx.doi.org/10.1002/ccr3.6775 | DOI Listing |
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