Methemoglobinemia (patient information)

Methemoglobinemia
Overview
What are the symptoms?
What are the causes?
When to seek urgent medical care?
Diagnosis
Treatment options
Where to find medical care for Methemoglobinemia?
What to expect (Outlook/Prognosis)?
Possible complications
Prevention
Methemoglobinemia On the Web
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Methemoglobinemia in the news
Blogs on Methemoglobinemia
Directions to Hospitals Treating Methemoglobinemia
Risk calculators and risk factors for Methemoglobinemia

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Methemoglobinemia is a blood disorder in which an abnormal amount of methemoglobin -- a form of hemoglobin -- is produced. Hemoglobin is the protein in red blood cells that carries and distributes oxygen to the body.

With methemoglobinemia, the hemoglobin can carry oxygen but is unable to release it effectively to body tissues.

What are the symptoms of Methemoglobinemia?

Symptoms of type 1 methemoglobinemia (erythrocyte reductase deficiency) include:

• Bluish coloring of the skin

Symptoms of type 2 methemoglobinemia (generalized reductase deficiency) include:

• Developmental delay
• Failure to thrive
• Intellectual disability
• Seizures

Symptoms of hemoglobin M disease include:

• Bluish coloring of the skin

Symptoms of acquired methemoglobinemia include:

• Bluish coloring of the skin
• Headache
• Fatigue
• Shortness of breath
• Lack of energy

What causes Methemoglobinemia?

This condition can be passed down through families (inherited or congenital). Or, it is caused by exposure to certain drugs, chemicals, or foods (acquired).

There are two forms of inherited methemoglobinemia. The first form is passed on by both parents. The parents usually do not have the condition themselves, but they carry the gene that causes the condition. It occurs when there is a problem with an enzyme called cytochrome b5 reductase.

There are two types of this form of methemoglobinemia:

• Type 1 (also called erythrocyte reductase deficiency) occurs when red blood cells lack the enzyme.
• Type 2 (also called generalized reductase deficiency) occurs when the enzyme doesn't work anywhere in the body.

The second form of inherited methemoglobinemia is called hemoglobin M disease. It is caused by defects in the hemoglobin protein itself. Only one parent needs to pass on the abnormal gene for the child to inherit the disease.

Acquired methemoglobinemia is more common than the inherited forms. It occurs in some people after they are exposed to certain chemicals and drugs, including:

• Anesthetics such as benzocaine
• Benzene
• Certain antibiotics (including dapsone and chloroquine)
• Nitrites (used as additives to prevent meat from spoiling)

The condition may also occur in infants who are very ill or who are fed too many vegetables containing nitrates (such as beets).

Where to find medical care for Methemoglobinemia?

Directions to Hospitals Treating Methemoglobinemia

Source

https://www.nlm.nih.gov/medlineplus/ency/article/000562.htm