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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

Acute Intermittent Porphyria (AIP) Gene Panel Test

The maximum days to obtain the report for the Acute Intermittent Porphyria (AIP) Gene Panel test is 14 days.

What are the prerequisites for the test Acute Intermittent Porphyria (AIP) Gene Panel

  • Patients suspected of having Acute Intermittent Porphyria (AIP) based on clinical symptoms and laboratory findings
  • Patients with a family history of AIP
  • Patients with unexplained abdominal pain, neuropathy, or psychiatric symptoms
  • Patients with unexplained elevations in urine porphobilinogen (PBG) and/or 5-aminolevulinic acid (ALA)

What are the measure values for the test Acute Intermittent Porphyria (AIP) Gene Panel

  • ALAD Gene Analysis - Normal
  • CPOX Gene Analysis - Normal
  • HMBS Gene Analysis - Normal
  • PBG-D Gene Analysis - Normal
  • PBG-D Urine Test - Normal
  • PBG-D Whole Blood Test - Normal
  • PPOX Gene Analysis - Normal
  • UROS Gene Analysis - Normal

What does this test Acute Intermittent Porphyria (AIP) Gene Panel identify?

  • Identification of mutations in the HMBS gene
  • Confirmation of a diagnosis of Acute Intermittent Porphyria (AIP)
  • Assessment of disease risk in family members of individuals with AIP
  • Guidance for treatment and management of AIP

Why is this test Acute Intermittent Porphyria (AIP) Gene Panel taken?

  • Reason for Test: The Acute Intermittent Porphyria (AIP) Gene Panel is taken to diagnose and confirm a suspected case of AIP in individuals who present with symptoms such as severe abdominal pain, neuropathy, and psychiatric manifestations.
  • Diagnostic Tool: This test is a diagnostic tool used to identify mutations in genes associated with AIP, including the HMBS gene.
  • Genetic Counseling: Results from the AIP Gene Panel can help in genetic counseling for affected individuals and their family members to understand the inheritance pattern and risk of passing on the condition.
  • Treatment Planning: Knowing the specific genetic mutations causing AIP can help in personalized treatment planning and management of the condition.

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