Orphanet: Diagnostic des lymphohistiocytoses h�r�ditaires et des d�fauts g�n�tiques entra�nant une susceptibilit� � l_EBV Panel
x

Search for a diagnostic test

* (*) mandatory field

Diagnosis of hereditary lymphohistiocytosis and genetic defects leading to susceptibility to EBV (Panel)

  • Centre d'Etudes des Dficits Immunitaires (CEDI)
  • Hpital Necker-Enfants Malades
  • 149 rue de Svres
  • 75743 PARIS
  • FRANCE
  • Director of laboratory : Pr Capucine PICARD
  • More information
  • Phone : 33 (0)1 44 49 58 96
  • Additional Phone : 33 (0)1 44 49 40 00
  • Fax : 33 (0)1 42 73 06 40
  • Website
  • Contact
Last update: February 2020

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
NGS sequencing (except WES)
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.