Microdeletion / Microduplication Syndromes
GTR Test Accession: Help GTR000568371.3
INHERITED DISEASESYNDROMIC DISEASEDYSMORPHOLOGY ... View more
Last updated in GTR: 2020-08-10
Last annual review date for the lab: 2023-07-28 LinkOut
At a Glance
Diagnosis; Mutation Confirmation
Chromosome 22q11.2 microduplication syndrome; 17q11.2 microduplication syndrome; 4p partial monosomy syndrome; ...
CLDN5 (22q11.21), CREBBP (16p13.3), CYP1A1 (15q24.1), DLG1 (3q29), DRC3 (17p11.2), ...
Molecular Genetics - Deletion/duplication analysis: Multiplex Ligation-dependent Probe Amplification (MLPA)
Not provided
The detection rates of alterations using Microdeletions/microduplications MLPA (P245) is …
Establish or confirm diagnosis
Ordering Information
Offered by: Help
Molecular Genetics and Cytogenetics, Clinical Laboratory Service
View lab's website
Specimen Source: Help
Who can order: Help
  • Licensed Physician
Test Order Code: Help
2752
Lab contact: Help
Marcela Lagos, MD, Lab Director
mlagos@med.puc.cl
+56 223548515
Contact Policy: Help
Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
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Recommended fields not provided:
Conditions Help
Total conditions: 28
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 39
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Multiplex Ligation-dependent Probe Amplification (MLPA)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis; Mutation Confirmation
Clinical validity: Help
The detection rates of alterations using Microdeletions/microduplications MLPA (P245) is 7% approximately in randomly selected Developmental delay (DD)/mental retardation (also described as intellectual disability) cases with/without malformations. Though MLPA cannot probe the whole genome like cytogenetic microarray, due to its ease and relative low cost it is an important technique … View more
View citations (1)
  • Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients. Boggula VR, et al. Indian J Med Res. 2014;139(1):66-75. PMID: 24604040.
Clinical utility: Help
Establish or confirm diagnosis
View citations (1)
  • Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients. Boggula VR, et al. Indian J Med Res. 2014;139(1):66-75. PMID: 24604040.

Variant Interpretation:
Are family members with defined clinical status recruited to assess significance of VUS without charge? Help
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Will the lab re-contact the ordering physician if variant interpretation changes? Help
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Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
For validation, 10 samples of patients with alterations in the critical regions covered by the SALSA® MLPA®Probemix P245 Microdeletion Syndromes kit were analyzed. All had been studied by CGH array. There was 100% concordance with the results previously detected with aCGH. Samples from healthy patients were also analyzed, no alterations … View more
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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