Autosomal dominant congenital metabolic disease

external

• Parents

  • Congenital metabolic disease
  • Autosomal dominant disorder

• Children

  • Porphyria
  • Acute intermittent porphyria
  • Renal Glycosuria
  • Hypokalaemic periodic paralysis
  • Alpha-1 antitrypsin deficiency
  • Gilbert syndrome
  • Liddle syndrome
  • Familial combined hyperlipidaemia
  • Familial hypertriglyceridaemia
  • Familial hypercholesterolaemia
  • Familial hypocalciuric hypercalcaemia
  • Maturity-onset diabetes of the young