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Requisites
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

The maximum days the report can be obtained for the test Disorder Of Osteopetrosis Related Test is 14 days.

What are the prerequisites for the test Disorder Of Osteopetrosis Related Test

  • Patients must have a suspected or confirmed diagnosis of osteopetrosis
  • Patients must have a medical history and physical examination consistent with osteopetrosis
  • Patients must have a referral from a healthcare provider
  • Patients should not have any contraindications to undergoing the test

What are the measure values for the test Disorder Of Osteopetrosis Related Test

Measure Value
Alkaline Phosphatase, Serum or Plasma Normal: 20-140 IU/L
Calcium, Total, Serum 8.5-10.5 mg/dL
Phosphorus, Serum 2.5-4.5 mg/dL
Parathyroid Hormone (PTH) 10-65 pg/mL
Vitamin D, 25-Hydroxy 20-50 ng/mL

What does this test Disorder Of Osteopetrosis Related Test identify?

Disorder Of Osteopetrosis Related Test

The Disorder Of Osteopetrosis Related Test is a diagnostic test that is used to identify and diagnose osteopetrosis, a rare genetic disorder characterized by abnormal bone growth and density. This test helps to determine the specific genetic mutations that may be causing the condition, as well as assess the severity of the disease.

Osteopetrosis can lead to a range of symptoms including bone fractures, bone pain, anemia, vision problems, and dental abnormalities. Early detection and diagnosis through this test can help in managing the symptoms and providing appropriate treatment.

Why is this test Disorder Of Osteopetrosis Related Test taken?

The Disorder Of Osteopetrosis Related Test is taken to diagnose and monitor individuals with osteopetrosis, a rare genetic disorder characterized by increased bone density and abnormal bone growth. This test helps healthcare providers determine the specific genetic mutation causing the condition and guide treatment decisions. It can also assess the severity of the disease and monitor response to treatment.

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