SPRED1 - Legius syndroom ¹

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Legius syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Legius syndrome

This product is also part of the following panels:

  • Hereditary cancer panel
  • Intellectual disability panel with genome wide CNV analysis
  • Lymphatic anomalies panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Noonan syndrome / RASopathy panel
  • panel neurofibromatosis type 1 / legius syndrome (NF1, SPRED1) ¹
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Skin disorders panel¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 609291
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 368
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Panel

panel neurofibromatosis type 1 / legius syndrome (NF1, SPRED1) ¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 520
View Add

panel neurofibromatosis type 1 / legius syndrome (NF1, SPRED1) ¹


€ 520
Add

panel neurofibromatosis type 1 / legius syndrome (NF1, SPRED1) ¹

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Legius syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Legius syndrome
  • Conditions > Skin > Neurofibromatosis
  • Conditions > Neurological > Neurofibromatosis
  • Conditions > Oncogenetics > Neurofibromatosis

Turnaround time
8 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA



€ 520
Add
Gene

SPRED1 - Legius syndroom ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 368
View Add

SPRED1 - Legius syndroom ¹


€ 368
Add