EpiSign Specific – Methylation analysis

Test code: AUA00003
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Epigenetic test: EpiSign Specific. Check the disclaimer, the latest syndromes and corresponding genes included in this panel (updates 31 March 2020). Specify the specific gene(s) of interest when ordering the test.

Indications

Suitable for patients with developmental delay, or with one or more overlapping features suggestive of one of the represented epigenetic signature conditions or imprinting disorders.

Detection

Methylation abnormalities may require additional targeted genetic testing. This test will not detect females with Fragile X (FMR1) expansions.

 

Genes

CDCA7, Chr17Q23.1-q24.2 dup NSD1, Chr21 trisomy, Chr4p16.13 del, Chr7q11.23 del, Chr7q11.23 dupl, EED, FRA12A, HELLS, SMARCC, UPD11 (IC1 and IC2), UPD7, ADNP, ARID1A, ARID1B, ATRX, BRWD3, CHD2, CHD7, CHD8, CREBBP, DIP2B, DNMT1, DNMT3A, DNMT3B, EHMT1, EP300, EZH2, FMR1, HIST1H1E, KANSL1, KAT6B, KDM5C, KDM6A, KMT2A, KMT2D, KMT5B, MEG3, NIPBL, NSD1, PHF6, SETD1B, SETD5, SMARCA2, SMARCA4, SMARCB1, SMC1A, SMC3, SMS, SNRPN, SRCAP, UBE2A, ZBTB24, ZNF711

Lab method

EpiSign, Methylation Analysis

Turnaround time

4 months

Location

Location AMC

Price  1.050,00

Category:

  • ADNP related syndrome
  • Alpha-thalassemia mental retardation (ATRX) syndrome (OMIM: 301040)
  • Angelman syndrome - AS (OMIM: 105830)
  • Autism, susceptibility to, 18 (OMIM: 615032)
  • BAFopathies
  • Börjeson-Forssman-Lehmann Syndrome (OMIM: 301900)
  • Cerebellar ataxia, deafness and narcolepsy a.d. ADCADN syndrome - DNMT1 (OMIM: 604121)
  • CHARGE syndrome (OMIM: 214800)
  • Claes-Jensen syndrome
  • Coffin Siris syndrome CSS (1-4, 8)
  • Cornelia de Lange syndrome
  • Down syndrome (OMIM: 602523)
  • Floating Harbor syndrome
  • Fragile X syndrome (Affected males only) (OMIM: 300624)
  • Genitopatellar syndrome
  • Kabuki syndrome
  • Kagami–Ogata syndrome UPD14 (OMIM: 608149)
  • Mental retardation, FRA12A type (OMIM: 136630)
  • Nicolaides-Baraitser (NCBRS) syndrome (OMIM: 601358)
  • Prader Willi syndrome - PWS (OMIM: 176270)
  • Silver-Russell syndrome - SRS (OMIM: 180860)
  • Sotos syndrome
  • Temple syndrome (OMIM: 616222)
  • Methylation disorders
  • Beckwith Wiedemann syndrome - BWS (OMIM: 130650)
  • Nicolaides Baraitser syndrome (OMIM: 601358)
  • Williams-Beuren syndrome WBS (OMIM: 194050)

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