Zweers E J, Erkelens D W
Academisch Ziekenhuis, afd. Interne Geneeskunde, Utrecht.
Ned Tijdschr Geneeskd. 1993 Jul 31;137(31):1570-3.
Familial mediterranean fever (or recurrent hereditary polyserositis) is a genetic disorder with an autosomal recessive pattern of inheritance which occurs mostly in patients with eastern Mediterranean origin. Two Dutch patients are described, a 25-year-old women and her 58-year-old father, who suffered from recurring abdominal complaints, fever, and increased erythrocyte sedimentation rate, without evidence of Middle Eastern ancestry or hyperimmunoglobulinemia D.
家族性地中海热(或复发性遗传性多浆膜炎)是一种常染色体隐性遗传模式的遗传性疾病,主要发生于起源于地中海东部的患者。本文描述了两名荷兰患者,一名25岁女性及其58岁父亲,他们反复出现腹部不适、发热和红细胞沉降率升高,且无中东血统或高免疫球蛋白D血症的证据。