Wiskott-Aldrich Syndrome (WAS): A Case Report in Mauritius and Review
Publish place: International Journal of Pediatrics، Vol: 3، Issue: 3
Publish Year: 1394
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_INJPM-3-3_002
تاریخ نمایه سازی: 20 مهر 1398
Abstract:
Wiskott-Aldrich is an X-lined recessive disorder typically characterized by thrombocytopenia, eczema and recurrent infections. We report the four year treatment progress of a six year old boy who initially presented with vesicular lesions over the trunk, upper and lower extremities and face and blood tinged stools at the age of 2 weeks. From the family pedigree, there were two suspected cases that were never successfully diagnosed with similar symptoms. The patient was diagnosed with Wiskott-Aldrich and underwent symptomatic treatment and treatment with prednisolone for the last four years. The platelet count over these four years was also studied.
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Authors
Kamleshun Ramphul
Department of Pediatrics, Shanghai Xin Hua Hospital affiliated to the Shanghai Jiao Tong University School of Medicine, China.
Sunjaye Ramjuttun
Department of Pediatrics, Sir Seewoosagur Ramgoolam National Hospital, Mauritius, China.
Vinita Poorun
Department of Pediatrics, Sir Seewoosagur Ramgoolam National Hospital, Mauritius, China.