Intracranial haemorrhage in siblings and ornithine transcarbamylase deficiency
Acta Paediatr Scand
.
1982 Jul;71(4):671-3.
doi: 10.1111/j.1651-2227.1982.tb09497.x.
Authors
J Amir
,
G Alpert
,
M Statter
,
A Gutman
,
S H Reisner
PMID:
7136688
DOI:
10.1111/j.1651-2227.1982.tb09497.x
No abstract available
Publication types
Case Reports
MeSH terms
Amino Acid Metabolism, Inborn Errors / genetics*
Ammonia / blood*
Cerebral Hemorrhage / genetics*
Humans
Infant, Newborn
Infant, Newborn, Diseases*
Male
Ornithine Carbamoyltransferase Deficiency Disease*
Substances
Ammonia