When the production of key enzymes is missing or deficient at birth, it causes disease. Most enzyme deficiencies are genetic disorders that lead to errors in metabolism. When there is an error in metabolism, the body cannot process chemicals efficiently, which can lead to dysfunction.
Enzymes are small proteins located inside cells that help support chemical reactions important for managing sugar, vitamin, protein, and fat levels which are essential for body functions. Thousands of different enzymes play crucial roles in metabolism.
Hundreds of different metabolic disorders can impact every system in the body. Determining which specific enzymes are deficient and understanding the processes that those enzymes control are key to defining the symptoms and available treatment approaches.
This article will discuss the different enzyme deficiencies, how they cause disease, and how they are treated.
Enzymes play an integral role in controlling metabolism within the body. The body is responsible for taking raw products from foods and turning them into useful products that support cellular and metabolic functions.
Chemical reactions within the body coordinate processes across all levels of the body, from controlling synaptic transmission in the brain to ensuring you have enough energy stored in your muscles for your next workout.
Enzymes help catalyze and speed up these chemical processes within the body. Most enzymes are small proteins that live within cells. Most enzymes have very specific functions in the body. Disruptions in even a single enzyme can lead to the development of metabolic diseases, also known as inborn errors of metabolism.
Since the body is responsible for processing many different molecules, each disorder is usually tied to a specific enzyme deficiency or the specific molecule that builds up within the body.
There are many different types of enzyme deficiencies and understanding the chemistry can be a daunting task. Enzyme deficiencies are often classified based on the metabolic pathway that they disrupt or the products that accumulate in the body.
A few enzyme deficiency disorders are:
Since metabolic disorders are present at birth, the symptoms often develop early in life. Most commonly, issues such as the inability to gain weight, irritability, and fatigue are present. Recurrent infections and an enlarged liver or spleen are other common symptoms experienced by those who are born with metabolic disorders.
If your child is consistently unable to gain weight or appears to remain sick despite ongoing treatment, your healthcare provider may consider testing for metabolic disorders.
Some metabolic disorders are not diagnosed until later in life. Glucose-6-phosphate dehydrogenase deficiency impacts red blood cells. Oftentimes, this disorder may not be significant until later stages of life, and then it is diagnosed.
Enzyme deficiencies are usually identified at birth or in early childhood. Every U.S. state performs newborn blood sample screening tests to identify and screen for metabolic disorders. Screening is conducted to identify the most common deficiencies and some rare deficiencies.
However, some deficiencies are delayed and may not become known until later in life. Assessment for metabolic disorders can be performed by a healthcare provider. It is most often performed using blood tests.
To better understand what enzyme deficiencies your state screens for, you can visit the department of health website for your state and review their newborn screening policies.
Treatment options for metabolic disorders are variable and depend on the underlying condition and process that are affected. In some cases, specific dietary changes are needed to reduce the effects of an enzyme disorder.
For example, in galactosemia , avoiding milk products is necessary since the body cannot process the molecule galactose, which is found in milk.
In other cases, for example with lysosomal storage disorders (which affect the metabolism of some fats and carbohydrates), options such as enzyme replacement therapy can be used.
Treating an enzyme disorder often requires specialized medical care. Since many enzyme disorders impact multiple regions of the body, you often need a multidisciplinary team of specialists who can coordinate together and recommend a comprehensive treatment plan.
Unfortunately, many enzyme disorders lack effective treatment options. Ongoing work aims to identify and validate new therapeutics to treat these conditions. Recent innovations have brought new therapies and treatments for conditions like Hunter's syndrome and more.
New genetic tools are being researched for metabolic disorders. Since many metabolic disorders result from specific gene defects, there is hope that the disease can be reversed by correcting the underlying gene.
Tools such as CRISPR-CAS9 have been used to treat blood disorders such as sickle cell disease, and there is ongoing research into using these techniques to treat other conditions. Inherited metabolic disorders are optimal targets for these interventions, and work is underway to bring these treatments to the clinic.
Metabolic disorders are inherited conditions present at birth that impact the body’s ability to process nutrients and eliminate wastes. Determining the specific enzymes that are deficient and the processes they control is necessary to determine the best treatments.
Some enzyme deficiencies have the option for enzyme replacement therapy while other deficiencies can be corrected by changing diet. Research is developing new treatments for enzyme deficiencies.
Enzyme deficiencies are rare diseases. However, there are many different types of metabolic deficiencies and they can be missed. If you suspect your child is showing signs of an enzyme deficiency, reach out to a healthcare provider.
Enzyme deficiencies are usually present when a child is born or revealed within the first few months of life. Children with enzyme deficiencies may have difficulty gaining weight, frequent infections, or abnormally enlarged organs.
Supplements such as vitamins and minerals may help support metabolism. The appropriate supplements for assisting someone with enzyme deficiency should be discussed with a healthcare provider. In some cases, specific supplements need to be added to ensure the body is able to metabolize appropriately.
Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy.
By Kevin James Cyr
Kevin is a physician-in-training at Stanford University School of Medicine with a focus in cardiovascular disease and bioengineering. His publications have earned international awards, and his work has been featured in major media outlets such as NBC News.
Verywell Health's content is for informational and educational purposes only. Our website is not intended to be a substitute for professional medical advice, diagnosis, or treatment.
Ⓒ 2024 Dotdash Media, Inc. — All rights reserved Verywell Health is part of the Dotdash Meredith publishing family.We and our 100 partners store and/or access information on a device, such as unique IDs in cookies to process personal data. You may accept or manage your choices by clicking below, including your right to object where legitimate interest is used, or at any time in the privacy policy page. These choices will be signaled to our partners and will not affect browsing data.
Store and/or access information on a device. Use limited data to select advertising. Create profiles for personalised advertising. Use profiles to select personalised advertising. Create profiles to personalise content. Use profiles to select personalised content. Measure advertising performance. Measure content performance. Understand audiences through statistics or combinations of data from different sources. Develop and improve services. Use limited data to select content. List of Partners (vendors)