Acute intermittent (hepatic) porphyria digital illustration

Acute intermittent (hepatic) porphyria Save


ICD-10 code: E80.21

Disease category: E80.2: Other and unspecified porphyria

Understanding Acute Intermittent (Hepatic) Porphyria

Acute Intermittent Porphyria (AIP) is a rare genetic disorder that affects the production of heme, a vital component of hemoglobin that carries oxygen in the blood. This type of porphyria is caused by a deficiency in the enzyme porphobilinogen deaminase (PBGD), which leads to the buildup of toxic substances called porphyrins in the body.

Individuals with AIP may experience a range of symptoms, including abdominal pain, vomiting, constipation, muscle weakness, and seizures. These symptoms may occur suddenly and may be triggered by factors such as stress, infection, hormonal changes, and certain medications.

Symptoms of Acute Intermittent Porphyria

The symptoms of AIP can vary widely from person to person and may include:

  1. Abdominal pain: This is the most common symptom of AIP and may be severe and constant or intermittent.
  2. Vomiting: Nausea and vomiting are common in individuals with AIP and may be severe.
  3. Constipation: This is a common symptom of AIP and may be caused by muscle weakness in the intestines.
  4. Muscle weakness: Weakness in the arms, legs, and back is common in individuals with AIP and may be severe.
  5. Seizures: Seizures may occur in individuals with AIP, particularly during an acute attack.
Diagnosis of Acute Intermittent Porphyria

Diagnosis of AIP may involve a range of tests, including:

  1. Urine tests: Urine tests can detect the presence of porphyrins in the body.
  2. Blood tests: Blood tests can measure the levels of PBGD and heme in the blood.
  3. Genetic testing: Genetic testing can confirm a diagnosis of AIP by identifying mutations in the PBGD gene.
  4. Electrolyte tests: Electrolyte tests can identify imbalances in the body’s salt and mineral levels.

If you or someone you know is experiencing symptoms of AIP, it is important to seek medical attention immediately. Early diagnosis and treatment can help to prevent complications and improve outcomes.

It is important to note that AIP is a rare condition, and not everyone who experiences these symptoms has AIP. Other conditions, such as gastrointestinal disorders, may present with similar symptoms. Therefore, it is important to consult with a healthcare provider for an accurate diagnosis and appropriate treatment

Treatment of Acute intermittent (hepatic) porphyria:

Treatment Options for Acute Intermittent Porphyria

Acute intermittent porphyria (AIP) is a rare genetic disorder that affects the production of heme, an essential component of hemoglobin. This condition can cause a range of symptoms, including abdominal pain, neuropsychiatric symptoms, and muscle weakness. While there is no cure for AIP, there are several treatment options that can...

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