Search for a diagnostic test
10 Result(s)
Caption
: Accreditation
= ;

GERMANY
Bayern
MÜNCHEN
Molecular diagnosis of immunodeficiency due to complement deficiency (C5, C6, C7 genes)
Pränatalmedizin München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

SWITZERLAND
Suisse Romande
GENÈVE
Diagnosis of complement mediated diseases (Panel)
Hôpitaux Universitaires de Genève HUG
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of predisposition to meningococcal infections : protein of complement common final pathway deficiency and properdin deficiency (C5, C6, C7, CFP, CFD, C8A, C8B, C8G, C9 genes)
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis, Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

BELGIUM
OOST-VLAANDEREN
GENT
Diagnosis of specific complement deficiencies (C3, C4, functional hemolytic test for the classical and alternative pathways (CH50 and AP50 test), serum titers of MBL) (only with blood drawn on site)
Ghent University Hospital - UZGent
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of hereditary immune deficiencies (Panel)
CHU Paris - Hôpital Necker-Enfants Malades
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

SPAIN
Madrid
MADRID
Diagnosis of immunodeficiency due to a late component of complement deficiency (C5 gene)
Hospital Universitario La Paz
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics, Immunology
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: Sanger sequencing

SPAIN
Comunidad Valenciana
PATERNA
Molecular diagnosis of immunodeficiency due to a late component of complements deficiency (C5 gene)
Sistemas Genómicos S.L.
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

FRANCE
AUVERGNE-RHONE-ALPES
GRENOBLE
Diagnosis of complement proteins in recurring meningococcal meningitis : complement proteins common final pathway deficiency (C5, C6, C7, C8, C9) and properdine deficiency
CHU de Grenoble site Nord - Institut de biologie et de pathologie
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

GERMANY
Baden-Württemberg
ULM
Immunological diagnosis of primary immunodeficiencies (PID) - Immunophenotyping including adhesion molecules
Klinik für Kinder- und Jugendmedizin des Universitätsklinikums Ulm
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

BELGIUM
OOST-VLAANDEREN
GENT