نتایج جستجو برای: alkaptonuria

تعداد نتایج: 375  

Journal: :Journal of clinical pathology 1966
K Valmikinathan N Verghese

Alireza Rafiei, Aref Hosseinian Amiri,

Background: Alkaptonuria (AKU) or ochronosis is a rare progressive degenerative arthropathy that results from deficiency of enzyme homogentisate 1,2 dioxygenase (HGD). The features include arthritis of the spine and in larger peripheral joints, with chondrocalcinosis. In this paper, we present a case of alkaptonuria in a 54 year old woman in Tehran, Iran. Case Presentation: A 54 year old woman ...

Journal: :Caspian journal of internal medicine 2012
Aref Hosseinian Amiri Alireza Rafiei

BACKGROUND Alkaptonuria (AKU) or ochronosis is a rare progressive degenerative arthropathy that results from deficiency of enzyme homogentisate 1,2 dioxygenase (HGD). The features include arthritis of the spine and in larger peripheral joints, with chondrocalcinosis. In this paper, we present a case of alkaptonuria in a 54 year old woman in Tehran, Iran. CASE PRESENTATION A 54 year old woman ...

Journal: :caspian journal of internal medicine 0
behnaz yousefghahari abbasali ahmadi ardeshir guran

background: alkaptonuria is a rare genetic disease leading to the accumulation of homogentesic acid in joint and ear cartilage, sclera and some other tissues causing significant morbidity in these patients. in this paper, we report three cases of alkaptonuria among the family or household members. case presentation: a 51-year-old man with mechanical low back and knee pain was referred to rheuma...

Journal: :The Netherlands journal of medicine 2003
J de Boer G W van Dam A A M Franken

A 60-year-old woman presented with typical features of alkaptonuria.

Journal: :Rheumatology 2018

2016
Farooq A. Rathore Saeed B. Ayaz Sahibzada N. Mansoor

Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is due to the lack of an enzyme homogentisate 1,2-dioxygenase, which results in an accumulation of homogentisic acid in different areas of the body, including sclera, skin, cardiac valves, articular cartilage of the large joints and intervertebral disks. We present two cases of alkaptonuria resulting...

Journal: :International Journal of Surgery & Surgical Procedures 2016

Journal: :Polskie Archiwum Medycyny Wewnetrznej 2016
Krzysztof Cieszyński Jakub Podgórny Adrianna Mostowska Paweł P Jagodziński Alicja E Grzegorzewska

Journal: :Indian journal of dermatology, venereology and leprology 2005
Shyam B Verma

Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxidase. This leads to the characteristic features like darkening of urine, ochronosis and arthropathy. Darkening of urine is one of the first symptoms noticed by the parents of the child suffering from this disorder. Ochronosis is seen in various organs like eyes, skin, tendons and joints. A case of ...

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