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Interdisciplinary CompetenceMolecular Diagnostics
Know how in the analysis of genetic material.
For the benefit of patients.

IllnessKleefstra-Syndrom, Differentialdiagnose

Summary

Short information

Comprehensive differential diagnostic panel for Kleefstra syndrome comprising 6 curated genes according to the clinical signs

ID
KP7120
Number of loci
Loci typeCount
Gen6
Accredited laboratory test
Examined sequence length
3,9 kb (Core-/Core-canditate-Genes)
33,5 kb (Extended panel: incl. additional genes)
Analysis Duration
on request
Test material
  • EDTA-anticoagulated blood (3-5 ml)
Diagnostic indications

NGS +

 

Loci panel

Gen

NameExon Length (bp)OMIM-GReferenz-Seq.Heredity
EHMT13897NM_024757.5AD
KMT2C14736NM_170606.3AD
MBD54485NM_018328.5AD
RAI15721NM_030665.4AD
TCF42016NM_001083962.2AD
UBE3A2559NM_130838.4AD

Informations about the disease

Synonyms
  • Alias: 9q- syndrome [DD: Down syndrome]
  • Alias: Chromosome 9q34.3 deletion syndrome
  • Angelman syndrome (UBE3A)
  • Kleefstra syndrome 1 (EHMT1)
  • Kleefstra syndrome 2 (KMT2C)
  • Mental retardation, AD 1 (MBD5)
  • Pitt-Hopkins syndrome (TCF4)
  • Smith-Magenis syndrome (RAI1)
Heredity, heredity patterns etc.
  • AD
OMIM-Ps
  • Multiple OMIM-Ps
ICD10 Code

Bioinformatics and clinical interpretation

No text defined