Frequent relapser minimal change nephrosis: an unrecognized X-linked disorder?

Case report

English

Awadalla NB, Teebi AS, Elzouki AY, Shaltout A.

Department of Paediatrics, Amiri Hospital and Faculty of Medicine, Raas, Kuwait.

Eur J Pediatr. 1989 Dec;149(3):205-7.

Abstract

We report three brothers who developed nephrosis between the age of 3-10 years. The parents were nonconsanguineous and of Arab descent. The mother’s sister had a son with a similar condition. Patients were steroid responders and frequent relapsers. Renal biopsies in the three brothers showed findings of minimal change nephrosis. This family may suggest the existence of an X-linked recessive nephrosis which provides further evidence for genetic heterogeneity of familial nephrosis.

Keywords: Frequent relapser minimal change nephrosis: an unrecognized X-linked disorder?

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