Alkaptonuria is a rare hereditary disorder which may result with arthropathy in multiple joints. Clinical findings are similar to degenerative joint diseases. It mostly involves the spine and extremities especially large joints. There is no consensus in the treatment of the disease. In this case we present the effect of physical therapy program in the treatment of back pain and a four year follow up results.Alkaptonüre bir çok eklemde artropatiye yol açabilen, nadir görülen herediter bir hastalıktır. Klinik bulgular dejeneratif hastalıklarla benzerlik göstermektedir. Ço- ğunlukla omurga ve ekstremitelerde büyük eklemleri tutar. Hastalığın tedavisinde kesinleşmiş bir görüş birliği mevcut değildir. Bu olguda, bel ağrısı tedavisind...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
INTRODUCTION- Alkaptonuria is a rare metabolic disorder affecting 1 in 250,000 to 1 million people w...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria is a rare hereditary disorder which may result with arthropathy in multiple joints. Cli...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Hospital files of alkaptonuria patients being followed up in Nutrition and Metabolism Unit of Hacett...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
The aim of the study was to study the quality of life of patients with alkaptonuria.Material and met...
AbstractThe current case report describes two cases of alkaptonuric ochronosis for anesthetic manage...
PubMed ID: 7641516Ochronotic arthropathy (spondylosis or peripheral arthropathy) is a late complicat...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Abstract The current case report describes two cases of alkaptonuric ochronosis for anesthetic manag...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
INTRODUCTION- Alkaptonuria is a rare metabolic disorder affecting 1 in 250,000 to 1 million people w...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria is a rare hereditary disorder which may result with arthropathy in multiple joints. Cli...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves ho...
Hospital files of alkaptonuria patients being followed up in Nutrition and Metabolism Unit of Hacett...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria is a rare hereditary metabolic disease of autosomal recessive inheritance, resulting fr...
The aim of the study was to study the quality of life of patients with alkaptonuria.Material and met...
AbstractThe current case report describes two cases of alkaptonuric ochronosis for anesthetic manage...
PubMed ID: 7641516Ochronotic arthropathy (spondylosis or peripheral arthropathy) is a late complicat...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Abstract The current case report describes two cases of alkaptonuric ochronosis for anesthetic manag...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
INTRODUCTION- Alkaptonuria is a rare metabolic disorder affecting 1 in 250,000 to 1 million people w...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...