Inborn error of metabolism

Inborn error of metabolism

Inborn errors of metabolism comprise a large class of genetic diseases involving disorders of metabolism. The majority are due to defects of single genes that code for enzymes that facilitate conversion of various substances (substrates) into others (products). In most of the disorders, problems arise due to accumulation of substances which are toxic or interfere with normal function, or to the effects of reduced ability to synthesize essential compounds. Inborn errors of metabolism are now often referred to as congenital metabolic diseases or inherited metabolic diseases, and these terms are considered synonymous.

The term inborn error of metabolism was coined by a British physician, Archibald Garrod (1857-1936), in the early 20th century (1908). He is known for the "one gene, one enzyme" hypothesis, which arose from his studies on the nature and inheritance of alkaptonuria. His seminal text, Inborn Errors of Metabolism was published in 1923.

Major categories of inherited metabolic diseases

Traditionally the inherited metabolic diseases were categorized as disorders of carbohydrate metabolism, amino acid metabolism, organic acid metabolism, or lysosomal storage diseases. In recent decades, hundreds of new inherited disorders of metabolism have been discovered and the categories have proliferated. Following are some of the major classes of congenital metabolic diseases, with prominent examples of each class. Many others do not fall into these categories. ICD-10 codes are provided where available.

Manifestations and presentations

Because of the enormous number of these diseases and wide range of systems affected, nearly every "presenting complaint" to a doctor may have a congenital metabolic disease as a possible cause, especially in childhood. The following are examples of potential manifestations affecting each of the major organ systems:

Diagnostic techniques

Because of the multiplicity of conditions, many different diagnostic tests are used for screening. An abnormal result is often followed by a subsequent "definitive test" to confirm the suspected diagnosis.

Common screening tests used in the last sixty years:

Specific diagnostic tests (or focused screening for a small set of disorders):

Newborn screening

Dozens of congenital metabolic diseases are now detectable by newborn screening tests, especially the expanded testing using mass spectrometry. This is an increasingly common way for the diagnosis to be made and sometimes results in earlier treatment and a better outcome.

Management

In the middle of the 20th century the principal treatment for some of the amino acid disorders was restriction of dietary protein and all other care was simply management of complications. In the last two decades, enzyme replacement, gene transfer, and organ transplantation have become available and beneficial for many previously untreatable disorders. Some of the more common or promising are listed.

  • Dietary restriction
  • Dietary supplementation or replacement
  • Vitamins
  • Intermediary metabolites, compounds, or drugs that facilitate or retard specific metabolic pathways
    • E.g.,
  • Dialysis
    • E.g.,
  • Enzyme replacement
    • E.g.,
  • Gene transfer
    • E.g.,
  • Bone marrow or organ transplantation
    • E.g.,
  • Treatment of symptoms and complications
    • E.g.,
  • Prenatal diagnosis and avoidance of pregnancy or abortion of an affected fetus
    • E.g.,

Resources

For clinicians and scientists in the field of inborn errors of metabolism, good resources include books by Scriver. Fernandes, Clarke, Blau (diagnosis), Blau (treatment) , Lyon, Nyhan, Hoffmann and Zschocke. Other ressources include genetests, orphanet, OMIM, Metab-L,societies such as the SSIEM, the SIMD and links therein. For medical students and clinicians looking for overviews of the field, such reviews can be found on pubmed and in good pediatric textbooks (e.g. articles by Saudubray, Ellaway, Raghuveer or Burton and textbooks by Hay or Behrman).

For patients, their families or other individuals seeking good information and support groups, the National Institutes of Health offers the office of rare diseases, genetics home reference, medlineplus and health information The National Human Genome Research Institute hosts an information center, a section for patients and the public and additional educational resources Support groups can be found at NORD, Genetic Alliance and Orphanet The genetic education center at the KUMC has many more useful links.

References

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