Glanville and Ross Bloom : Case of Renal Tubular Osteomalacia ( Dent Type

نویسنده

  • H. J. GLANVILLE
چکیده

FIG. 1.-Pseudo-fractures of first metacarpals in 1957. FIG. 2.-Gomplete healing of metacarpal fractures in 1958. FIG. 3.-Metacarpal fractures still healed in January 1964. No subperiosteal erosions have developed as a result of the hyperparathyroidism, indicating that this is the type that affects plasma levels without producing specific bone disease. FIG. 4.-Femoral pseudo-fractures (arrowed) in June 1957. The fractures healed completely with treatment. FIG. 5.-Recurrence of femoral Looser zones in July 1963 after reduction in dose of dihydrotachysterol.

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

Hypophosphataemic Osteomalacia in the Adult with Defective Renal Tubular Function. a Report of Four Cases, with Special Mention of the Effects of Massive Doses of Vitamin D (calciferol).

Osteomalacia in the adult is usually the result of malabsorption of calcium by the intestinal tract. Sometimes, however, it is due to a defect in the convoluted tubules of the kidney: either a tubular acidosis or a defective reabsorption of phosphorus by the proximal cells of the tubules. This condition may form part of the syndrome first described by Fanconi (1936) in the child, and later by G...

متن کامل

Dent–Wrong disease and other rare causes of the Fanconi syndrome

Dent-Wrong disease, an X-linked recessive disorder of the proximal tubules, presents with hypercalciuria, nephrocalcinosis, nephrolithiasis, renal insufficiency, low-molecular-weight proteinuria, rickets and/or osteomalacia. Dent and Friedman initially characterized the disorder in 1964 following studies of two patients with rickets who presented with hypercalciuria, hyperphosphaturia, proteinu...

متن کامل

Distal renal tubular acidosis, hypokalemic paralysis, nephrocalcinosis, primary hypothyroidism, growth retardation, osteomalacia and osteoporosis leading to pathological fracture: a case report.

Renal tubular acidosis (RTA) is a constellation of syndromes arising from different derangements of tubular acid transport. Recent advances in the biology of urinary acidification have allowed us to discern various molecular mechanisms responsible for these syndromes. RTA often presents as renal stone disease with nephrocalcinosis, ricket/osteomalacia and growth retardation in children with ult...

متن کامل

The Fanconi syndrome; metabolic studies on treatment.

The association of rickets or osteomalacia with a variety of renal tubular defects, probably congenital, has been called by many different names such as resistant rickets, Fanconi syndrome, and hyperchloraemic acidosis with nephrocalcinosis. They have been classified by I)ent (1952) into six main types according to the various combinations of recognisal)Ie defects of tubule function. The Fancon...

متن کامل

Primary Sjogren's Syndrome Presenting as Osteomalacia

Background: The most common renal disease in Sjogren’s syndrome (SjS) is tubulo-interstitial nephritis, which is responsible for renal tubular acidosis type 1 (RTA-1) in around 20% of patients. Osteomalacia rarely occurs as the first manifestation of a renal tubule disorder due to a connective tissue disease such as SjS. Results and conclusion: We report a 47-year-old woman with tubular acidosi...

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   شماره 

صفحات  -

تاریخ انتشار 2007