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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

The maximum days the report can be obtained for the test Seckel Syndrome Gene Panel is 21 days.

What are the prerequisites for the test Seckel Syndrome Gene Panel

  • Requisition form filled out and signed by a licensed healthcare provider
  • Patient's informed consent form signed
  • 2-5 mL of blood collected in an EDTA tube
  • Patient's demographic information
  • Any relevant clinical information or family history

What are the measure values for the test Seckel Syndrome Gene Panel

  • ATR gene sequencing
  • CDC6 gene sequencing
  • CENPJ gene sequencing
  • CEP152 gene sequencing
  • CEP63 gene sequencing
  • CENPJ gene sequencing
  • CEP152 gene sequencing
  • CEP63 gene sequencing
  • CEP152 gene sequencing
  • CEP63 gene sequencing

What does this test Seckel Syndrome Gene Panel identify?

  • This test identifies mutations in genes associated with Seckel syndrome, including ATR, CENPJ, CEP152, CEP63, NIN, and more.
  • Seckel syndrome is a rare genetic disorder characterized by severe growth retardation, microcephaly, intellectual disability, and distinct facial features.
  • The gene panel test helps in the diagnosis of Seckel syndrome by detecting mutations in the genes known to be involved in the development of the condition.
  • Identifying these mutations can provide important information for genetic counseling, family planning, and potential treatment options for individuals affected by Seckel syndrome.

Why is this test Seckel Syndrome Gene Panel taken?

Seckel Syndrome Gene Panel Test

The Seckel Syndrome Gene Panel Test is taken to diagnose Seckel syndrome, a rare genetic disorder characterized by growth retardation, microcephaly (small head size), and intellectual disability. This test analyzes a panel of genes known to be associated with Seckel syndrome to identify any mutations or variations that may be causing the condition.

By identifying the specific genetic cause of Seckel syndrome, healthcare providers can provide more personalized and targeted treatment options for individuals affected by this disorder. Additionally, genetic testing can help in genetic counseling and family planning for individuals at risk of passing on the syndrome to their children.

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