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Searched: Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Sequencing Panel with CNV Detection
Search Results
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Test CodeMethodPrice7545Sequencing with CNV PGxome$2190
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Test CodeMethodPrice7857Sequencing with CNV PG-Select$1890
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…testing eligibility criteria and must be ordered by a qualified healthcare provider. Clinical Features Generalized arterial calcification of infancy (also referred as Idiopathic infantile arterial calcification) is a rare infantile onset…
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Test CodeMethodPrice15157Sequencing with CNV PG-Select$990
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…Disorders Dyskeratosis Congenita Ectodermal Dysplasia Ehlers-Danlos Syndrome Epidermolysis Bullosa Fraser Syndrome Generalized Arterial Calcification of Infancy Hermansky-Pudlak Syndrome Hypopigmentation Ichthyosis Marfan Syndrome Neurofibromatosis…
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…Congenital Heart Disease Disorders of Fatty Acid Oxidation Dystrophinopathies Ectodermal Dysplasia Ehlers-Danlos Syndrome Fabry Disease Generalized Arterial Calcification of Infancy Hereditary Hemorrhagic Telangiectasia Heterotaxy Holt-Oram…
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…Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum (PXE) via the ABCC6 Gene Test Code Method Price 7857 Sequencing with CNV PG-Select $1890 Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum…
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…Panel Test Code Method Price 10449 Sequencing with CNV PG-Select $990 Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Panel Test Code Method Price 7545 Sequencing with CNV PGxome $2190 Generalized, Partial…
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…, severe, debilitating calcification disorders: ENPP1 Deficiency and ABCC6 Deficiency. Both these disorders can manifest as generalized arterial calcification of infancy (GACI) type 1 in infancy and then autosomal recessive hypophosphatemic…
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…$990 Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Panel Test Code Method Price 7545 Sequencing with CNV PGxome $2190 Generalized Arterial Calcification of Infancy via the ENPP1 Gene Test Code Method Price 15157…
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Test CodeMethodPrice3251Sequencing with CNV PGxome$990
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Test CodeMethodPrice7947Sequencing with CNV PGxome$1290
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Test CodeMethodPrice10383Sequencing with CNV PGxome$1290
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Test CodeMethodPrice15423Sequencing with CNV PGxome$1390
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Test CodeMethodPrice12027Sequencing with CNV PGxome$990
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…, a condition which has been called Generalized Arterial Calcification of Infancy Type 1 or GACI in infancy, and/or Autosomal Recessive Hypophosphatemic Rickets Type 2 (ARHR2) post infancy. Changes in the ABCC6 gene can cause ATP binding…
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Test CodeMethodPrice3253Sequencing with CNV PGxome$990
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…in two rare, severe calcification disorders, known as ENPP1 Deficiency and ABCC6 Deficiency, respectively, (sometimes called generalized arterial calcification of infancy [GACI] and autosomal recessive hypophosphatemic rickets type 2 [ARHR2…
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice15487Sequencing with CNV PGxome$1290
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