Menahem S, Adams A
Department of Cardiology, Royal Children's Hospital, Melbourne, Australia.
Acta Paediatr Scand. 1989 Sep;78(5):800-3. doi: 10.1111/j.1651-2227.1989.tb11151.x.
A neonate is described whose clinical condition rapidly and irreversibly deteriorated on day two. He developed a profound acidosis, hypoglycaemia and a shock-like syndrome. The infant was centrally cyanosed and had a systolic murmur from a moderately severe pulmonary valve stenosis and a small atrial septal defect. The overwhelming acidosis was inconsistent with the severity of the congenital heart defects and as no infection was found a metabolic cause was sought. Liver tissue obtained at autopsy shortly after death on day four, showed deficiencies of fructose-1, 6-biphosphatase and aldolase.