Liver cell transplantation was performed in a child with urea cycle disorder poorly equilibrated by conventional therapy as a bridge to transplantation. A 14-month-old boy with ornithine transcarbamylase (OTC) deficiency received 0.24 billion viable cryopreserved cells/kg over 16 weeks. Tacrolimus and steroids were given as immunosuppressive treatment while the patient was kept on the pre-cell transplant therapy. Mean blood ammonia level decreased significantly following the seven first infusions, while urea levels started to increase from undetectable values. After those seven infusions, an ammonium peak up to 263 microg/dL, clinically well tolerated, was observed. Interestingly, blood urea levels increased continuously to reach 25 mg/dL, ...
Ornithine transcarbamylase deficiency (OTCD) is a monogenic disease of ammonia metabolism in hepatoc...
Hepatocyte transplantation is an investigational alternative to orthotopic liver transplantation to ...
none10noThe urea cycle is the final pathway for nitrogen metabolism. Urea cycle disorders (UCDs) inc...
Hyperammonemia, abnormalities in plasma amino acids and abnormalities of standard liver functions we...
Urea cycle disorders (UCDs) are inherited metabolic diseases causing hyperammonemia by defects in ur...
Ornithine transcarbamylase (OTC) deficiency is an X chromosome-linked disorder causing hyperammonemi...
A male patient, born in 1999, was diagnosed with ornithine transcarbamylase deficiency as neonate an...
We describe 10 females with ornithine transcarbamylase (OTC) deficiency and liver dysfunction, revea...
Background & Aims Patient-derived human induced pluripotent stem cells (hiPSCs) differentiated into...
BACKGROUND Acute liver failure (ALF) has been reported in ornithine transcarbamylase deficiency (...
BACKGROUND & AIMS Patient-derived human induced pluripotent stem cells (hiPSCs) differentiated in...
Urea cycle (UC) is the main pathway of ammonium removal. A deficiency in any of the five classical e...
Background HHH syndrome is a rare autosomal recessive disorder of the urea cycle, caused by a defici...
BACKGROUND Acute liver failure (ALF) has been reported in ornithine transcarbamylase deficiency (OTC...
BACKGROUND & AIMS: Donor cell engraftment with expression of enzyme activity is the goal of liver ce...
Ornithine transcarbamylase deficiency (OTCD) is a monogenic disease of ammonia metabolism in hepatoc...
Hepatocyte transplantation is an investigational alternative to orthotopic liver transplantation to ...
none10noThe urea cycle is the final pathway for nitrogen metabolism. Urea cycle disorders (UCDs) inc...
Hyperammonemia, abnormalities in plasma amino acids and abnormalities of standard liver functions we...
Urea cycle disorders (UCDs) are inherited metabolic diseases causing hyperammonemia by defects in ur...
Ornithine transcarbamylase (OTC) deficiency is an X chromosome-linked disorder causing hyperammonemi...
A male patient, born in 1999, was diagnosed with ornithine transcarbamylase deficiency as neonate an...
We describe 10 females with ornithine transcarbamylase (OTC) deficiency and liver dysfunction, revea...
Background & Aims Patient-derived human induced pluripotent stem cells (hiPSCs) differentiated into...
BACKGROUND Acute liver failure (ALF) has been reported in ornithine transcarbamylase deficiency (...
BACKGROUND & AIMS Patient-derived human induced pluripotent stem cells (hiPSCs) differentiated in...
Urea cycle (UC) is the main pathway of ammonium removal. A deficiency in any of the five classical e...
Background HHH syndrome is a rare autosomal recessive disorder of the urea cycle, caused by a defici...
BACKGROUND Acute liver failure (ALF) has been reported in ornithine transcarbamylase deficiency (OTC...
BACKGROUND & AIMS: Donor cell engraftment with expression of enzyme activity is the goal of liver ce...
Ornithine transcarbamylase deficiency (OTCD) is a monogenic disease of ammonia metabolism in hepatoc...
Hepatocyte transplantation is an investigational alternative to orthotopic liver transplantation to ...
none10noThe urea cycle is the final pathway for nitrogen metabolism. Urea cycle disorders (UCDs) inc...