Volume 18, Number 6 (Jan- Feb 2011)                   JSSU 2011, 18(6): 570-577 | Back to browse issues page


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Najafi F. Senior Loken Syndrome. JSSU. 2011; 18 (6) :570-577
URL: http://jssu.ssu.ac.ir/article-1-1336-en.html

Abstract:   (7740 Views)
The etiology of ESRD under the age of 20 almost is the inherited kidney disease or congenital disorders of urinary tract. NPHP/ medullary cystic disease includes a group of tubulo- genetic kidney disorders. NPHP is the cause of 15-20% ESRD in children and adolescents. The extra renal manifestations include: oculomotor Apraxia(Cogan syndrome), mental retardation, retinitis pigmentosa, (Senior- Loken syndrome) liver fibrosis and skeletal disorders. Recently, on the basis of genetics and type of the protein product of these mutations, NPHP is divided to 6 types. The presented case is a 17 year old boy with end stage renal disease that he has been managed with hemodialysis. As the patient has polyuria and disturbance in vision from childhood and on physical examination he had retinitis pigmentosa and horizontal nystagmus with a history of chronic kidney disease in his 12 years old sister, and familial marriage between his parents, we suggest NPHP4 for the patient.
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Type of Study: case report | Subject: General
Received: 2011/01/24

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