Disorders  Enzyme deficiency Clinical features Gene/locus   Chromosome  
GSDIa/ Von Gierke Glucose-6-phosphatase Severe hypoglycaemia, Hepatomegaly, elevated lactate, lipids G6PC gene 17q21 [42]
GSD Ib Glucose-6-phosphate translocase Same as GSD Ia with neutropenia and impaired neutrophil function SLC37A4 11q23.3 [43]
GSD IIIa/Cori Amylo,1,6 glucosidase (Liver and muscle) Hepatomegaly, muscle weakness, hypoglycaemia, hyperlipidaemia AGL 1p21.2 [44]
GSD IIIb Amylo,1,6 glucosidase (Liver only) Hepatomegaly, hypoglycaemia, hyperlipidaemia AGL 1p21.2 [44]
GSDVI/Hers disease Liver phosphorylase Hepatomegaly and mild to moderate hypoglycaemia PYGL 14q22.1 [46]
GSD IXb Phosphorylase kinase (Liver and muscle) Hepatomegaly and mild hypoglycaemia on prolonged fasting PHKB 16q12.1 [48,49]
GSD IXc Phosphorylase kinase deficiency, Liver/Testis Hepatomegaly, recurrent hypoglycaemia, Liver cirrhosis PHKG2 16p11.2 [48,49]
GSD 0 Glycogen synthetase deficiency Hypoglycaemia and hyperketonaemia GYS2 12p12.1 [51]
Table 2: Glycogen storage disorders presenting with hypoglycaemia