DENMARK

Medical Genetics Laboratory Center
The Kennedy Institute – National Eye Clinic
Gl. Landevej 7                                                                               
Glostrup        
Denmark                       
DK-2600
Dr. Nina Horn
labcontact@kisoe.org
Cytogenetic analysis  of Incontinentia pigmenti
X-inactivation test for Incontinentia pigmenti

FRANCE

Centre de Génétique
Hôpital d'Enfants, 10 bd Maréchal de Lattre de Tassigny
Dijon
France
21000
Dr. Laurence Faivre
Dr. Christel Thauvin-Robinet 
christel.thauvin@chu-dijon.fr  
Molecular diagnosis of Orofaciodigital syndrome, type I

Department of Medical Genetics
Purpan Hospital
Pavillon Lefebvre                                                                        
Toulouse 
FRANCE               
31024
Prof. Alain Hovnanian
alain.hovnanian@toulouse.inserm.fr
Molecular diagnosis of Hypohidrotic ectodermal dysplasia

MAGEC centre, Dermatology department 
Necker Enfants Malades Hospital, Assistance Publique,
149 rue de Sèvres                                                                              
Paris                
France                           
75015
Prof. Christine Bodemer
Dr. Hadj Rabia          
Hadj-Rabia@necker.fr
Cell biology of Hypohidrotic ectodermal dysplasia
Cell biology of Hypohidrotic ectodermal dysplasia, with immune deficiency
Cell biology of Hypohidrotic ectodermal dysplasia, with immune deficiency, osteopetrosis and lymphoedema
Cell biology of Hypohidrotic ectodermal dysplasia, with hypothyroidism and ciliary dyskinesia
Cell biology of Incontinentia pigmenti
Histology/Immunohistochemistry of Incontinentia pigmenti
Histology/Immunohistochemistry of Mucoepithelial dysplasia, hereditary
Electron microscopy of Mucoepithelial dysplasia, hereditary
Molecular diagnosis of Hypohidrotic ectodermal dysplasia
Molecular diagnosis of Hypohidrotic ectodermal dysplasia, with immune deficiency
Molecular diagnosis of Hypohidrotic ectodermal dysplasia, with immune deficiency, osteopetrosis and lymphoedema
Molecular diagnosis of Incontinentia pigmenti

GERMANY

Center for Human Genetics Freiburg
Heinrich-von-Stephan-Str. 5
Freiburg
Germany
79100
Prof. Jürgen Kohlhase 
jkohlhase@humangenetik-freiburg.de 
Molecular diagnosis of Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome)
Molecular diagnosis of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)
Molecular diagnosis of Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome (EEC syndrome)
Molecular diagnosis of Limb-mammary syndrome
Molecular diagnosis of Rapp-Hodgkin syndrome
Molecular diagnosis of Rothmund-Thomson syndrome
Molecular diagnosis of Ulnar-mammary syndrome

Center for Human Genetics Regensburg
Universitätsklinikum, D3
Franz-Josef-Strauss-Allee 11
Regensburg
Germany
93053
Dr. Ute Hehr 
ute.hehr@humangenetik-regensburg.de 
Molecular analysis of Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome)
Molecular analysis of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)
Molecular analysis of Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome (EEC syndrome)
Molecular analysis of Hypohidrotic ectodermal dysplasia
Molecular analysis of Limb-mammary syndrome
Molecular analysis of Rapp-Hodgkin syndrome

Center for Medical Genetics
Caprivistr. 30
Osnabrueck
Germany
49076
Dr. Anna Gencik
Dr. Peter Jagiello and Dr. Heinz D. Gabriel 
zmg@gmx.net 
Molecular diagnosis of Hypohidrotic ectodermal dysplasia

Department of Dermatology
University Hospital
Von-Esmarch-Str. 58
Muenster
Germany
48149
Prof. Heiko Traupe
Dr. Vinzenz Oji
Vinzenz.oji@ukmuenster.de
Histology/Immunohistochemistry of Incontinentia pigmenti

EM-Labor
Universitats-Hautklinik
Vossstr. 2                                                                               
Heidelberg                  
Germany                          
69115
Dr. Ingrid Hausser
Ingrid.Hausser@med.uni-heidelberg.de
Histology/Immunohistochemistry of Hidrotic ectodermal dysplasia (Clouston syndrome)
Histology/Immunohistochemistry of Hypohidrotic ectodermal dysplasia
Histology/Immunohistochemistry of Hypohidrotic ectodermal dysplasia, with immune deficiency
Histology/Immunohistochemistry of Hypohidrotic ectodermal dysplasia, with immune deficiency, osteopetrosis and lymphoedema
Histology/Immunohistochemistry of Hypohidrotic ectodermal dysplasia, with hypothyroidism and ciliary dyskinesia
Histology/Immunohistochemistry of Hypohidrotic ectodermal dysplasia with hypothyroidism and agenesis of the corpus callosum
Electron microscopy of Ectodermal dysplasia, skin fragility syndrome

Institute of Medical Genetics
Charité - Universitätsmedizin Berlin
Austenburger Platz 1
Berlin
D-13353 Germany
Prof. Stefan Mundlos
Dr. Hartmut Peters 
hartmut.peters@charite.de 
Molecular diagnosis of Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome)
Molecular diagnosis of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)
Molecular diagnosis of Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome (EEC syndrome)
Molecular diagnosis of Limb-mammary syndrome
Molecular diagnosis of Rapp-Hodgkin syndrome
Molecular diagnosis of Ulnar mammary syndrome

University Medical Center Freiburg
Department of Dermatology     
Hauptstraße 7  
79104 Freiburg i. Br.
Germany
Prof. Leena  Bruckner-Tuderman
Daniela Kirstein
eb-zentrum@haut.ukl.uni-freiburg.de
Molecular analysis of Incontinentia pigmenti

HUNGARY

Department of Dermatology, Venerology and Dermatooncology
Semmelweis University
Mária str. 41
Budapest
Hungary
H-1085
Prof Sarolta Kárpáti
Dr. Marta Medvecz-Csikós 
csimar@bor.sote.hu 
Histology/Immunohistochemistry of Ectodermal dysplasias
Electron microscopy of Ectodermal dysplasias

ITALY

CEINGE Biotecnologie Avanzate SCarl (Center for Genetic Engineering)
via Comunale Margherita 482
Naples
Italy
80145
Dr. Caterina Missero 
missero@ceinge.unina.it 
Molecular analysis of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)

Department of Specialistic and Experimental Clinical Medicine,
Division of Clinical Dermatology
University of Bologna
via Massarenti 1
Bologna
40138 Italy
Prof. Claudio Varotti
Dr. Beatrice Passarini 
beatrice.passarini@unibo.it 
Histology/Immunohistochemistry of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)
Histology/Immunohistochemistry of Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED)
Histology/Immunohistochemistry of Cleft lip/palate-ectodermal dysplasia syndrome
Histology/Immunohistochemistry of Clouston syndrome
Histology/Immunohistochemistry of Dyskeratosis congenita
Histology/Immunohistochemistry of Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome (EEC syndrome)
Histology/Immunohistochemistry of Focal dermal hypoplasia syndrome
Histology/Immunohistochemistry of Hypohidrotic ectodermal displasia
Histology/Immunohistochemistry of Incontinentia pigmenti
Histology/Immunohistochemistry of Orofaciodigital syndrome type I
Histology/Immunohistochemistry of Rapp-Hodgkin syndrome
Histology/Immunohistochemistry of Rothmund-Thomson syndrome
Histology/Immunohistochemistry of Trichodental syndrome

Human Molecular genetics
Institute of Genetics and Biophysics
Via P.Castellino 111
Naples
Italy
80131
Dr. Catello Polito
Dr. Matilde Valeria Ursini
ursini@igb.cnr.it
Molecular analysis of Hypohidrotic ectodermal dysplasia, with immune deficiency
Molecular analysis of Hypohidrotic ectodermal dysplasia, with immune deficiency, osteopetrosis and lymphoedema
Molecular analysis of Incontinentia pigmenti

Laboratorio di Biologia molecolare e Genetica "Cante di Montevecchio"
Associazione Cante di Montevecchio
Via Negusanti s.n.
Fano (PU)
61032 Italy
Dr. Luigia Varriale 
luigia.varriale@genetica-cante.it 
Molecular diagnosis of hypohidrotic ectodermal dysplasia

TIGEM - Telethon Institute of Genetics and Medicine
Via Pietro Castellino 111
Naples
Italy
80131
Prof. Andrea Ballabio
Dr. Brunella Franco 
franco@tigem.it 
Molecular diagnosis of Orofaciodigital sindrome type I

SPAIN

Medical Genetics Unit
Sistemas Genomicos
Ronda G Marconi, 6. Technology Park of Valencia
E46980 Paterna (Valencia)
SPAIN
Dr. Javier Garcia-Planells
javier.garcia@sistemasgenomicos.com
Molecular analysis of Incontinentia pigmenti

Unidad de Medicina Molecular
Fundación Pública Gallega de Medicina Genómica
Hospital Clínico Universitario - Choupana Sn
Santiago de Compostela
Spain
15883
Dr. Fernando Dominguez
Dr. Lourdes Loidi 
Lloidi@Usc.Es  
Molecular diagnosis of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy syndrome (APECED)

SWITZERLAND

Division of Human Genetics / Dept. of Paediatrics
Inselspital / University of Bern
Freiburgstrasse
Bern
Switzerland
CH-3010
Prof. Sabina Gallati
Dr. Franziska Joncourt 
franziska.joncourt@dkf.unibe.ch 
Molecular diagnosis of Hidrotic ectodermal dysplasia (Clouston syndrome)
Molecular diagnosis of Rothmund-Thomson syndrome

Medical Molecular Genetics
University of Zurich, Institute of Medical Genetics
Schorenstrasse 16
Schwerzenbach
Switzerland
8603
Prof. Wolfgang Berger 
berger@medgen.unizh.ch  
Molecular diagnosis of Incontinentia Pigmenti

Molecular Diagnostic Laboratory, Medical Genetics
Geneva University Hospital
1 rue Michel-Servet
Geneva
Switzerland
1211
Dr. Michael Morris
Dr. Bouchardy Isabelle 
isabelle.bouchardy@medecine.unige.ch 
Molecular diagnosis of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy syndrome (APECED)
Molecular diagnosis of Hypohidrotic ectodermal dysplasia

THE NETHERLANDS

Clinical Genetics/DNA diagnostics
University Medical Centre Groningen
Hanzeplein 1                                                                              
9700RB Groningen           
The Netherlands
Dr. Henny Lemmink
H.H.Lemmink@medgen.umcg.nl or secr-dna@medgen.umcg.nl
Molecular diagnosis of Hypohidrotic ectodermal dysplasia
Molecular diagnosis of Hypohidrotic ectodermal dysplasia, with immune deficiency
Molecular diagnosis of Hypohidrotic ectodermal dysplasia, with immune deficiency, osteopetrosis and lymphoedema
Molecular diagnosis of Incontinentia pigmenti

UNITED KINGDOM

Genetics Laboratories
Addenbrooke's NHS Trust
Kefford House, Maris Lane
Trumpington, Cambridge
UK
CB2 2FF
Dr. Joanne Whittaker
Rebecca Treacy 
becky.treacy@addenbrookes.nhs.uk 
Molecular diagnosis of Incontinentia Pigmenti 

Genetic Skin Disease Group Division of Genetics and Molecular Medicine
St John’s Institute of Dermatology  St Thomas’ Hospital                  
Lambeth Palace Road                           
London SE1 7EH
UK
Prof. John McGrath
Dr. Suzanne Clements
Suz_clements@hotmail.com
Histology/Immunohistochemistry of Ectodermal dysplasia, skin fragility syndrome
Electron microscopy of Ectodermal dysplasia, skin fragility syndrome
Molecular analysis of Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome)
Molecular analysis of Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome (AEC syndrome)
Molecular analysis of Ectodermal dysplasia, skin fragility syndrome (McGrath syndrome)
Molecular analysis of Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome (EEC syndrome)
Molecular analysis of Limb-mammary syndrome
Molecular analysis of Rapp-Hodgkin syndrome