BackgroundIncreased homogentisic acid (HGA) causes ochronosis. Nitisinone decreases HGA. The aim was to study the effect of nitisinone on the ochronosis progression.MethodsPhotographs of the eyes and ears were acquired from patients attending the National Alkaptonuria Centre (NAC) at V-1 (pre-baseline visit), V0 (baseline visit when 2 mg nitisinone was commenced), and yearly at V1, V2, and V3 visits. Photographs were inspected for evolution of ochronotic pigment and also scored categorically to derive eye, ear, and combined ochronosis scores. An ear cartilage biopsy was also carried out at V0 and one year after V3 (V4) and ochronotic pigment was assessed and quantitated. Visits were compared for changes in pigment. Fasting blood and 24-hour...
Purpose: Alkaptonuria is a rare autosomal recessive form of osteoarthropathy resulting from deficien...
BackgroundAlthough changes in the tyrosine pathway during nitisinone therapy are known, a complete c...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Background Alkaptonuria (AKU) is present from birth, yet clinical effects are considered to appear l...
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published...
Alkaptonuria (AKU) is an ultrarare autosomal recessive disorder resulting from a deficiency of homog...
Alkaptonuria is a rare genetic disorder characterized by a high level of circulating (and urine) hom...
Background Alkaptonuria is a rare, debilitating autosomal recessive disorder affecting tyrosine meta...
Question Does Nitisinone prevent the clinical progression of the Alkaptonuria? Findings In this obse...
Background: Alkaptonuria (AKU) is present from birth, yet clinical effects are considered to appear ...
Ochronosis is the process in alkaptonuria (AKU) that causes all the debilitating morbidity. The proc...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
QUESTION: Does Nitisinone prevent the clinical progression of the Alkaptonuria? FINDINGS: In this ob...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
Changes in the phenylalanine (PHE)/tyrosine (TYR) pathway metabolites before and during homogentisic...
Purpose: Alkaptonuria is a rare autosomal recessive form of osteoarthropathy resulting from deficien...
BackgroundAlthough changes in the tyrosine pathway during nitisinone therapy are known, a complete c...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Background Alkaptonuria (AKU) is present from birth, yet clinical effects are considered to appear l...
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published...
Alkaptonuria (AKU) is an ultrarare autosomal recessive disorder resulting from a deficiency of homog...
Alkaptonuria is a rare genetic disorder characterized by a high level of circulating (and urine) hom...
Background Alkaptonuria is a rare, debilitating autosomal recessive disorder affecting tyrosine meta...
Question Does Nitisinone prevent the clinical progression of the Alkaptonuria? Findings In this obse...
Background: Alkaptonuria (AKU) is present from birth, yet clinical effects are considered to appear ...
Ochronosis is the process in alkaptonuria (AKU) that causes all the debilitating morbidity. The proc...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
QUESTION: Does Nitisinone prevent the clinical progression of the Alkaptonuria? FINDINGS: In this ob...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
Changes in the phenylalanine (PHE)/tyrosine (TYR) pathway metabolites before and during homogentisic...
Purpose: Alkaptonuria is a rare autosomal recessive form of osteoarthropathy resulting from deficien...
BackgroundAlthough changes in the tyrosine pathway during nitisinone therapy are known, a complete c...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...