A 4-year-old girl presented at our clinic with autistic-like symptoms, aggressivity and occasional hyperactivity. She had no history of neurologic or physical symptoms. Her condition was diagnosed as pervasive developmental disorder not otherwise specified, according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV). She received pharmacologic (thioridazine), educational and speech therapy. During this process, a urea cycle disorder was also identified, namely, ornithine transcarbamylase deficiency and arginase deficiency, because of the high level of ammonia in the patient's bloodstream, the high level of organic acids in the 24-hour urine collection and the constant presence of slow mult...
Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to t...
We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) presenting w...
Background: Disorders of urea cycle constitute approximately 50% of severe neonatal hyperammonemia. ...
A 4-year-old girl presented at our clinic with autistic-like symptoms, aggressivity and occasional h...
Congenital ornithine transcarbamylase deficiency (OTCD, OMIM 311250, Xp21.1) in humans results in hy...
Infantile autism is behaviorally defined as neurodevelopment disorder, beginning at a very young sta...
Argininemia or hyperargininemia is a urea cycle disorder caused by deficiency of the enzyme arginase...
Inborn errors of urea synthesis lead to an accumulation of ammonia in blood and brain, and result in...
Ammonia; It is a toxic molecule for the central nervous system resulting from the catabolism of prot...
Background: Argininosuccinic aciduria, the second most common urea cycle disorder (UCD) is due to ar...
Autism is a complex and life-long behavioural disorder of unknown aetiology. Recent reports have ind...
Three children with the late onset form of argininosuccinic aciduria are presented. The first two ar...
Three children with the late onset form of argininosuccinic aciduria are presented. The first two ar...
p.202-205We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) pre...
We report the case of a child with partial biotinidase deficiency and autistic developmental disorde...
Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to t...
We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) presenting w...
Background: Disorders of urea cycle constitute approximately 50% of severe neonatal hyperammonemia. ...
A 4-year-old girl presented at our clinic with autistic-like symptoms, aggressivity and occasional h...
Congenital ornithine transcarbamylase deficiency (OTCD, OMIM 311250, Xp21.1) in humans results in hy...
Infantile autism is behaviorally defined as neurodevelopment disorder, beginning at a very young sta...
Argininemia or hyperargininemia is a urea cycle disorder caused by deficiency of the enzyme arginase...
Inborn errors of urea synthesis lead to an accumulation of ammonia in blood and brain, and result in...
Ammonia; It is a toxic molecule for the central nervous system resulting from the catabolism of prot...
Background: Argininosuccinic aciduria, the second most common urea cycle disorder (UCD) is due to ar...
Autism is a complex and life-long behavioural disorder of unknown aetiology. Recent reports have ind...
Three children with the late onset form of argininosuccinic aciduria are presented. The first two ar...
Three children with the late onset form of argininosuccinic aciduria are presented. The first two ar...
p.202-205We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) pre...
We report the case of a child with partial biotinidase deficiency and autistic developmental disorde...
Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to t...
We describe three unrelated individuals, two males (ages 35 and 9) and a female (age 8) presenting w...
Background: Disorders of urea cycle constitute approximately 50% of severe neonatal hyperammonemia. ...