An Unusual Case of Proteinuria

نویسنده

  • M. M. Syddiq Hussain
چکیده

to me by a medical student for examination of her blood and urine. She said she was now putting on weight but to me she appeared thin and pale. She has had three live births and one abortion. The first and the second children are now 22 and 20 years old respectively; the third was an abortion at the seventh month and the fourth died at the age of 7 years. This happened about 6 years ago. Soon after the death of the last child she began to have irregular and scanty menses, and finally once in every 5 to 6 months. She approached a hakim for treatment. Her urine at this time was perfectly normal looking. Soon after she started the treatment she felt palpita'tion and giddiness. To use her own words she did not feel very certain about herself. Then she had itching of the hands and feet, followed by boils. The quantity of urine also began to be diminished and it was irritating. Next she went to her son who was also a hakim. He prescribed some other medicine which gave rise to intractable diarrhoea. Three months after she started the latter treatment the urine became milky, more so, if she drank milk and ate more meat. During this period she had an attack of urticaria which disappeared after some medication. Some distant relations of hers whom she used to visit

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Glomerular Disorder of Unknown Etiology in a Child with Unusual Course

A 3-year-old girl was presented with periorbital edema, hypertension, proteinuria, and hematuria. She recovered clinically after 9 days with normal urinalysis. During the follow-up, she developed recurrent episodes of nephrotic syndrome. The kidney biopsy revealed mild mesangial proliferation and a low dose of prednisolone could effectively control the disease.Iran J Med Sci 2005; 30(1): 38-40....

متن کامل

Fanconi Anemia Concurrent with an Unusual Thumb Polydactyly: A Case Report

  This case report presents a case of Fanconi’s Anemia with an unusual thumb polydactyly in a 2-year old boy. The extra thumb had no nail, nail bed and distal phalanx. The extra thumb had no active motion.The duplication of the thumb occurred at the carpometacarpal joint but its morphology did not match with any classification described for thumb polydactyly. Although his thumb polydactyly was ...

متن کامل

An unusual case of bilateral maxillary and mandibular supernumerary teeth

بعلت چاپ همزمان در دو مجله متن مقاله حذف گردید

متن کامل

Tinea incognito simulating dermatitis herpetiformis: An unusual case report

Tinea incognito is a dermatophyte infection of the skin with an atypical presentation attributed to inappropriate treatment with immunosuppressive medications. In thi

متن کامل

Imerslund-Grasbeck Syndrome: A Case Report

Introduction: Megaloblasc anemia is an uncommon problem in childhood most frequently associated with vitamin deficiency or gastrointesnal disease. The common causes of megaloblasc anemia are vitamin B12 (cobalamin) deficiency and folic acid deficiency. Familial selecve malabsorpon of vitamin B12 associated with proteinuria firstly was described by Imerslund (1960) and Grasbeck et al (1960)...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 76  شماره 

صفحات  -

تاریخ انتشار 1941