Wiskott-Aldrich Syndrome (WAS): A Case Report in Mauritius and Review
عنوان مقاله: Wiskott-Aldrich Syndrome (WAS): A Case Report in Mauritius and Review
شناسه ملی مقاله: JR_INJPM-3-3_002
منتشر شده در شماره 3 دوره 3 فصل در سال 1394
شناسه ملی مقاله: JR_INJPM-3-3_002
منتشر شده در شماره 3 دوره 3 فصل در سال 1394
مشخصات نویسندگان مقاله:
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.
خلاصه مقاله:
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.
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.
کلمات کلیدی: wiskott-aldrich, eczema, microthrombocytopenia
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/940514/