Connective Tissue Laboratory

Personnel

Director: Anne De Paepe, PhD, MD, Head of the Department
Phone: +32/9/332.36.03
Fax: +32/9/33259
Email: connective_tissue@cmgg.be
Sofie Symoens, PhD, Lab supervisor
Phone: +32/9/332.36.03
Email: connective_tissue@cmgg.be
Bert Callewaert, PhD, MD, Clinical Geneticist/Pediatrician
Phone: +32/9/332.36.03
Email: connective_tissue@cmgg.be
Paul Coucke, PhD, Lab Director
Phone: +32/9/332.36.03
Fax: +32/9/332.65.49
Email: connective_tissue@cmgg.be
Julie De Backer, PhD, MD, Clinical Geneticist/Cardiologist
Phone: +32/9/332.36.03
Email: connective_tissue@cmgg.be
Fransiska Malfait, PhD, MD, Clinical Geneticist, Rheumatologist
Phone: +32/9/332.36.03
Email: connective_tissue@cmgg.be
Olivier Vanakker, PhD, MD, Clinical Geneticist/Pediatrician
Phone: +32/9/332.36.03
Email: connective_tissue@cmgg.be

Conditions and tests

89 conditions/phenotypes with 89 tests
Enter text to narrow down the list

Achondrogenesis type II2 tests
ALDH18A1-related de Barsy syndrome11 tests
Aneurysm-osteoarthritis syndrome11 tests
Aortic aneurysm, familial thoracic 411 tests
Aortic aneurysm, familial thoracic 611 tests
Aortic aneurysm, familial thoracic 710 tests
Aortic aneurysm, familial thoracic 810 tests
Aortic valve disease 110 tests
Arrhythmogenic right ventricular dysplasia 111 tests
Arterial calcification, generalized, of infancy, 14 tests
Arterial calcification, generalized, of infancy, 24 tests
Arterial tortuosity syndrome10 tests
Autosomal recessive cutis laxa type 2B11 tests
Autosomal recessive inherited pseudoxanthoma elasticum4 tests
Avascular necrosis of femoral head, primary, 12 tests
Bethlem myopathy 1A5 tests
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency4 tests
Brain small vessel disease 1 with or without ocular anomalies3 tests
Brittle cornea syndrome 13 tests
Brittle cornea syndrome 23 tests
Cardiac valvular dysplasia, X-linked9 tests
Congenital contractural arachnodactyly10 tests
Cutis laxa with osteodystrophy11 tests
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies11 tests
Cutis laxa, autosomal dominant 119 tests
Cutis laxa, autosomal dominant 211 tests
Cutis laxa, autosomal recessive1 test
Cutis laxa, autosomal recessive, type 1A11 tests
Cutis laxa, autosomal recessive, type 1B19 tests
Cutis laxa, X-linked11 tests
Ectopia lentis 1, isolated, autosomal dominant4 tests
Ectopia lentis 2, isolated, autosomal recessive4 tests
Ectopia lentis et pupillae4 tests
Ehlers-Danlos syndrome progeroid type11 tests
Ehlers-Danlos syndrome, classic type3 tests
Ehlers-Danlos syndrome, classic type, 13 tests
Ehlers-Danlos syndrome, dermatosparaxis type11 tests
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type11 tests
Ehlers-Danlos syndrome, kyphoscoliotic type 111 tests
Ehlers-Danlos syndrome, musculocontractural type11 tests
Ehlers-Danlos syndrome, musculocontractural type 211 tests
Ehlers-Danlos syndrome, spondylocheirodysplastic type11 tests
Ehlers-Danlos syndrome, spondylodysplastic type, 211 tests
Ehlers-Danlos syndrome, type 412 tests
Geroderma osteodysplastica11 tests
Kniest dysplasia2 tests
Larsen-like syndrome, B3GAT3 type11 tests
Legg-Calve-Perthes disease2 tests
Loeys-Dietz syndrome 111 tests
Loeys-Dietz syndrome 211 tests
Loeys-Dietz syndrome 411 tests
Marfan syndrome11 tests
MASS syndrome11 tests
Menkes kinky-hair syndrome11 tests
Microspherophakia4 tests
Moyamoya disease 511 tests
Multiple epiphyseal dysplasia, Beighton type2 tests
Multisystemic smooth muscle dysfunction syndrome11 tests
Namaqualand hip dysplasia2 tests
Osteogenesis imperfecta15 tests
Osteogenesis imperfecta type I3 tests
Osteogenesis imperfecta type III3 tests
Osteogenesis imperfecta with normal sclerae, dominant form3 tests
Osteogenesis imperfecta, perinatal lethal3 tests
Otospondylomegaepiphyseal dysplasia, autosomal dominant4 tests
Otospondylomegaepiphyseal dysplasia, autosomal recessive2 tests
Platyspondylic dysplasia, Torrance type2 tests
Porencephaly 23 tests
Pseudoxanthoma elasticum, forme fruste4 tests
PYCR1-related de Barsy syndrome11 tests
RIN2 syndrome2 tests
Shprintzen-Goldberg syndrome11 tests
Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures11 tests
Spondyloepiphyseal dysplasia congenita2 tests
Spondyloepiphyseal dysplasia with metatarsal shortening2 tests
Spondylometaphyseal dysplasia2 tests
Spondyloperipheral dysplasia2 tests
Stickler syndrome1 test
Stickler syndrome type 14 tests
Stickler syndrome type 24 tests
Stickler syndrome, type I, nonsyndromic ocular4 tests
Stiff skin syndrome11 tests
Supravalvar aortic stenosis19 tests
Type II Collagenopathies1 test
Ullrich congenital muscular dystrophy 1A5 tests
Vitamin K-dependent clotting factors, combined deficiency of, type 14 tests
Weill-Marchesani syndrome 110 tests
Weill-Marchesani syndrome 2, dominant11 tests
Wrinkly skin syndrome11 tests

List of services

This lab has no services.

List of certifications/licenses

Certifications

ISO15189, Number: 351-MED, Expiration date: 2021-09-10

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.