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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 for obtaining the report for the test Ectodermal Dysplasia Gene Panel is 21 days.

What are the prerequisites for the test Ectodermal Dysplasia Gene Panel

  • Consultation with a medical geneticist or genetic counselor
  • Confirmation of clinical diagnosis of ectodermal dysplasia
  • Family history assessment
  • Signed informed consent for genetic testing

What are the measure values for the test Ectodermal Dysplasia Gene Panel

  • EDA Gene Sequencing: $300
  • EDAR Gene Sequencing: $250
  • EDARADD Gene Sequencing: $200
  • WNT10A Gene Sequencing: $150
  • TP63 Gene Sequencing: $350

What does this test Ectodermal Dysplasia Gene Panel identify?

  • Ectodermal Dysplasia Gene Panel identifies mutations in genes associated with ectodermal dysplasia, a group of genetic disorders that affect the development of ectodermal structures such as hair, teeth, nails, and sweat glands.
  • This panel typically includes analysis of genes such as EDA, EDAR, TP63, and others that are known to be involved in ectodermal dysplasia.
  • Identifying mutations in these genes can help diagnose individuals with ectodermal dysplasia and provide information about the specific subtype of the disorder they may have.
  • Results from this panel can also be used for genetic counseling, family planning, and potentially targeted treatment options for individuals with ectodermal dysplasia.

Why is this test Ectodermal Dysplasia Gene Panel taken?

The Ectodermal Dysplasia Gene Panel test is taken to diagnose individuals suspected of having ectodermal dysplasia, a group of genetic disorders that affect the development of ectodermal structures such as hair, teeth, nails, and sweat glands. This panel test analyzes multiple genes associated with different types of ectodermal dysplasia to identify specific genetic mutations that may be causing the symptoms in the individual. The results of this test can help in confirming a diagnosis, providing personalized treatment options, and offering genetic counseling to affected individuals and their families.

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