Idiopathic Fanconi Syndrome without Cystinosis
نویسندگان
چکیده
منابع مشابه
Light chain tubulopathy without Fanconi syndrome.
A 59-year-old white male was found to have mild proteinuria and renal insufficiency during a life insurance test in 2003. His serum creatinine has been stable at 1.6mg/dl since then. His 24 h urine protein was 720mg in 2003 and 861mg in 2006. Urinalysis showed 1þ protein with inactive sediment. His ANA, hepatitis B surface antigen, hepatitis C antibody and serum cryoglobulin were all negative. ...
متن کاملIdiopathic intracranial hypertension in cystinosis.
OBJECTIVES To report a high frequency of idiopathic intracranial hypertension (IIH) in patients with cystinosis and to speculate on the relationship between these two disorders. STUDY DESIGN Retrospective case series and review of the literature regarding risk factors for the development of IIH in cystinosis. RESULTS Eight patients with cystinosis had documented papilledema, normal neuroima...
متن کاملIdiopathic Hypereosinophilic Syndrome
Idiopathic hypereosinophilic syndrome is a multisystem disease with peripheral blood eosinophilia of at least 6 months duration, multiple organ system involvement, and no evidence for other known causes of eosinophilia. It is characteristically a disease of middle-aged men, often has a poor prognosis and is seldom found during childhood. Heart dicsease, characterized by endomyocardial fibrosis ...
متن کاملFanconi or not Fanconi? Lowe syndrome revisited.
R enal Fanconi syndromes are both clinically challenging and physiologically fascinating. The diagnosis requires a certain index of suspicion to correctly identify the clinical symptomatology and pursue the appropriate laboratory evaluations. With regard to the pathophysiology, the renal proximal tubule is the site of action. Through a complex and coordinated machinery of luminal and basolatera...
متن کاملPlasma and muscle free carnitine deficiency due to renal Fanconi syndrome.
Plasma and urine free and acyl carnitine were measured in 19 children with nephropathic cystinosis and renal Fanconi syndrome. Each patient exhibited a deficiency of plasma free carnitine (mean 11.7 +/- 4.0 [SD] nmol/ml) compared with normal control values (42.0 +/- 9.0 nmol/ml) (P less than 0.001). Mean plasma acyl carnitine in the cystinotic subjects was normal. Four subjects with Fanconi syn...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1969
ISSN: 0035-9157
DOI: 10.1177/003591576906211p112