Ornithine transcarbamylase deficiency: Neuropathologic changes acquired in utero

1986 ◽  
Vol 108 (6) ◽  
pp. 942-945 ◽  
Author(s):  
F. Filloux ◽  
J.J. Townsend ◽  
C. Leonard
Keyword(s):  
In Utero ◽  
Ornithine Transcarbamylase ◽  
Ornithine Transcarbamylase Deficiency

scholarly journals Ornithine transcarbamylase deficiency: A possible risk factor for thrombosis

2009 ◽  
Vol 53 (1) ◽  
pp. 100-102 ◽  
Author(s):  
Lakshmi Venkateswaran ◽  
Fernando Scaglia ◽  
Valerie McLin ◽  
Paula Hertel ◽  
Oleg A. Shchelochkov ◽  
...  
Keyword(s):  
Risk Factor ◽  
Ornithine Transcarbamylase ◽  
Ornithine Transcarbamylase Deficiency

scholarly journals Hepatocellular Adenoma in a Patient with Ornithine Transcarbamylase Deficiency

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Lin Cheng ◽  
Yajuan Liu ◽  
Wenjing Wang ◽  
J. L. Merritt ◽  
Matthew Yeh
Keyword(s):  
Liver Damage ◽  
English Language ◽  
Scientific Literature ◽  
Hepatocellular Adenoma ◽  
Ornithine Transcarbamylase ◽  
Ornithine Transcarbamylase Deficiency ◽  
Otc Deficiency

Ornithine transcarbamylase (OTC) deficiency is an X-linked recessive disorder that leads to hyperammonemia and liver damage. Hepatocellular adenoma in OTC deficiency patients has not been previously described. Here we report the first such case to be described in the English language scientific literature.

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