by EBSCO Medical Review Board


Inherited metabolic diseases are a group of disorders that result in missing or defective enzymes. The enzyme problems can lead to:

  • A build up of harmful items that the enzymes would normally breakdown
  • The body not being able to fully breakdown food for use in the cells

There are thousands of these disorders.


These diseases are caused by a problem with the genes that determine how specific enzymes are made. The genes are passed on to a child from one or both parents.

Genetic Material
Chromosome DNA
Copyright © Nucleus Medical Media, Inc.

Risk Factors

This problem is more common in people with:

  • Ashkenazi Jewish, Finnish, or Dutch ancestry
  • A family history of metabolic disorders
  • A brother or sister who died at birth or who had sudden infant death syndrome
  • Parents who are related to each other


Problems in infants happen shortly after birth and can be severe. They may be:

  • Being very sleepy
  • Weak muscles
  • Feeding problems
  • Vomiting
  • Rapid breathing
  • Muscle spasms or twitches
  • Problems with hearing or sight
  • Not meeting milestones
  • Seizures
  • Problems with the liver, such as a yellowing of the skin or the whites of the eyes
  • Problems with the heart or kidney

Problems can also be mild and found after 1 year of age. A child may have:

  • Trouble with balance
  • Movements that they cannot control
  • Loss of feeling or movement
  • Muscle tightening
  • Behavior or mental health problems
  • Loss of developmental skills or language


Most disorders are found during prenatal testing and newborn screening. In others, the doctor will ask about your child's symptoms and health history. A physical exam will be done.

Blood tests will be done to look for causes. Skin, blood, and urine tests will be done to confirm the diagnosis and look for the enzyme that is causing the problem.

Other tests may also be done, such as:

  • Eyesight and hearing tests
  • Neuropsychological testing to measure brain function
  • MRI scan to view images
  • Lumbar puncture to test the fluid around the brain and spine
  • Tissue biopsy
  • Electromyography (EMG) to measure the electrical activity of the muscles
  • Other special tests of the heart, liver, and kidneys


Some infants and children will need care right away, such as IV fluids and medicines. Ongoing treatment will depend on the type of disorder. Some choices are:

  • Dietary changes, such as taking vitamins and not eating certain foods
  • Physical therapy to help with strength, flexibility, and range of motion
  • Medicine to:
    • Decrease the harmful items that the missing enzymes would normally breakdown
    • Replace missing enzymes
  • A stem cell transplant to encourage the body to make the missing enzyme
  • Dialysis to filter blood when the kidneys are not able to do so

Infants and children who are not helped by these methods may need surgery.


There are no known guidelines to prevent these disorders.


Children Living with Inherited Metabolic Disorders 

Society for Inherited Metabolic Disorders 


The Canadian Mucopolysaccharide & Related Diseases Society 

Health Canada 


Acute porphyria. EBSCO DynaMed website. Available at: Accessed March 2, 2021.

Ezgu F. Inborn Errors of Metabolism. Adv Clin Chem. 2016;73:195-250.

Inherited metabolic disorder. National Information Center for Metabolic Diseases (CLIMB) website. Available at: Accessed March 2, 2021.

Karim Z, Lyoumi S, et al. Porphyrias: A 2015 update. Clin Res Hepatol Gastroenterol. 2015 Sep;39(4):412-425.

Rice GM, Steiner RD. Inborn Errors of Metabolism (Metabolic Disorders). Pediatr Rev. 2016 Jan;37(1):3-17

Revision Information

  • Reviewer: EBSCO Medical Review Board Kari Kassir, MD
  • Review Date: 12/2020
  • Update Date: 03/02/2021