Two sisters were diagnosed with childhood systemic lupus erythematous

المؤلفون المشاركون

Nasrawi, Ala Jumah Munji
al-Sunbli, Hibah Yahya

المصدر

Kufa Medical Journal

العدد

المجلد 18، العدد 2 (31 ديسمبر/كانون الأول 2022)، ص ص. 41-44، 4ص.

الناشر

جامعة الكوفة كلية الطب

تاريخ النشر

2022-12-31

دولة النشر

العراق

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

We are herein reporting two female siblings with childhood-onset Systemic Lupus Erythematosus (SLE).

The children were diagnosed as having SLE in reverse birth order at ages 2 and 6 years.

Younger sister's initial symptoms were serositis, proteinuria, and hemolytic anemia with laboratory findings of hypocomplementemia and positive ANA/anti-dsDNA antibody.

After 18 months, the older sister presented with high-grade fever, arthralgia proteinuria, oral mucous ulcer, butterfly rash, and positive ANA/anti-dsDNA antibody.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Sunbli, Hibah Yahya& Nasrawi, Ala Jumah Munji. 2022. Two sisters were diagnosed with childhood systemic lupus erythematous. Kufa Medical Journal،Vol. 18, no. 2, pp.41-44.
https://search.emarefa.net/detail/BIM-1494070

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Sunbli, Hibah Yahya& Nasrawi, Ala Jumah Munji. Two sisters were diagnosed with childhood systemic lupus erythematous. Kufa Medical Journal Vol. 18, no. 2 (Dec. 2022), pp.41-44.
https://search.emarefa.net/detail/BIM-1494070

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Sunbli, Hibah Yahya& Nasrawi, Ala Jumah Munji. Two sisters were diagnosed with childhood systemic lupus erythematous. Kufa Medical Journal. 2022. Vol. 18, no. 2, pp.41-44.
https://search.emarefa.net/detail/BIM-1494070

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 44

رقم السجل

BIM-1494070