Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic

Alternative Names

  • PCKDC
  • PCK1 Deficiency, Cytosolic
  • PEPCK Deficiency, Cytosolic
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WHO-ICD-10 version:2010

Endocrine, nutritional and metabolic diseases

Metabolic disorders

OMIM Number

261680

Mode of Inheritance

Autosomal recessive

Gene Map Locus

20q13.31

Description

Cytosolic phosphoenolpyruvate carboxykinase deficiency causes a defect in gluconeogenesis that results in a 'biochemical signature' of fasting hypoglycemia with high tricarboxylic acid cycle intermediate excretion, particularly of fumarate. Other biochemical anomalies that may be seen during metabolic crisis include ketonuria, dicarboxylic aciduria, and urea cycle dysfunction. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
261680.1.1OmanFemaleYesYes Epileptic encephalopathy; Intellectual d...NM_002591.4:c.961+1G>AHomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Proband from "family...
261680.1.2OmanFemaleYesYes HypoglycemiaNM_002591.4:c.961+1G>AHomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Sister of 261680.1.1
261680.1.3OmanMaleYesYes Hypoglycemia; Elevated circulating hepat...NM_002591.4:c.961+1G>AHomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Brother of 261680.1....
261680.2.1OmanFemaleYesYes Hypoglycemia; Lactic acidosis; Vomiting;...NM_002591.4:c.574T>CHomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Proband from "family...
261680.2.2OmanFemaleYesYes Lactic acidosis; Vomiting; Nonketotic hy...NM_002591.4:c.574T>CHomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Sister of 261680.2.1
261680.3.1United Arab EmiratesMaleNo Hypoglycemia; Vomiting; Hepatomegaly; Me...NM_002591.4:c.1268C>THomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Proband from "family...
261680.4OmanMaleYes Encephalopathy; Seizure; Respiratory dis...NM_002591.4:c.1268C>THomozygousAutosomal, RecessiveAl Busaidi et al. 2023 Proband from "family...
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