Number of Panel Genes:
11
Nonsyndromic hypotrichosis is an inherited disorder affecting the structure and growth of hair. The phenotype of hypotrichosis varies from almost normal hair to complete hair loss. All body hair can be affected or it can be limited to scalp hair. The findings may include hair loss, thinning of the hair, woolly hair, slow hair growth, and thin, fragile, and dry hair.
read moreTests Available
11 Panel Genes: APCDD1, CDSN, DSG4, HR, KRT25, KRT71, KRT74, LIPH, LPAR6, RPL21, SNRPE
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Next Generation Sequencing
$1,100
Test Code: 5306
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Deletion / Duplication
$990
Test Code: 5307
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NGS/Del Dup Comprehensive
$1,300
Test Code: 5308
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Test Details
Technical Information
Panel Genes:
APCDD1, CDSN, DSG4, HR, KRT25, KRT71, KRT74, LIPH, LPAR6, RPL21, SNRPE
Disease Groups:
Skin, Tooth, Nail and Hair Disorders
Billing
CPT Codes:
81479 x 1
Ordering
SKU:
5306 Turnaround Time:
Typically 2 to 4 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens:
- Whole blood: purple-top (EDTA) tube, minimum of 3 ml
- Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
- Fibroblasts: 2 confluent T-25 flasks
- Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens:
- Cultured cells: 2 confluent T-25 flasks derived from amnio or CVS samples
- Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
Shipping:
Ship all specimen types at room temperature by overnight courier. Do not freeze.