CTGT Announces 15 New Diagnostic Tests

June 25, 2012 - Connective Tissue Gene Tests (CTGT) is pleased to announce 15 new tests for inherited connective tissue disorders.

New Tests:

DISORDER SEQ DEL/DUP
Apert syndrome X  
Beare-Stevenson cutis gyrata syndrome (BSTVS) X  
Bent bone dysplasia syndrome (BBDS) X  
Craniosynostosis, type 1 (CRS1) X  
Crouzon syndrome X  
Crouzon syndrome with acanthosis nigricans (CAN) X  
FGFR1, FGFR2 and FGFR3 related craniosynostosis panel X  
FGFR2 related craniosynostosis X  
Jackson-Weiss syndrome (JWS) X  
Marfan syndrome (MFS), Loeys-Dietz syndrome, type 1A (LDS1A) and Loeys-Dietz syndrome, type 1B (LDS1B) X  
Metaphyseal anadysplasia 1 (MANDP1) X  
Muenke syndrome (MNKES) X  
Pfeiffer syndrome X  
Saethre-Chotzen syndrome (SCS) X  
Spondyloepimetaphyseal dysplasia, Missouri type (SEMD, Missouri type) X  

The new tests may be ordered using the requisition forms on CTGT's web site. As new tests are added frequently, CTGT advise clients to regularly download the latest requisition forms from the Requisition Forms page on the web site.

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