Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome

American Journal of Obstetrics and Gynecology

Volumn 193, Issue 5, 2005, Pages 1743-1745

  Esser, Tilman ^a   Rogalla, Patrick ^a   Bamberg, Christian ^a   Kalache, Karim D ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

Apert Syndrome; Prenatal diagnosis; Three dimensional ultrasonography

Indexed keywords

ACROCEPHALOSYNDACTYLY; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; FEMALE; FETUS; GESTATIONAL AGE; HUMAN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SKULL; THREE DIMENSIONAL IMAGING;

ACROCEPHALOSYNDACTYLIA; ADULT; FEMALE; HUMANS; ULTRASONOGRAPHY, PRENATAL;

EID: 27544490288     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajog.2005.07.043     Document Type: Article

References (2)

1. S. von Gernet, A. Golla, Y. Ehrenfels, S. Schuffenhauer, and J.D. Fairley Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery Clin Genet 57 2000 137 139
2. G. Boog, C. Le Vaillant, N. Winer, A. David, M.P. Quere, and M.F. Nomballais Contribution of tridimensional sonography and magnetic resonance imaging to prenatal diagnosis of Apert syndrome at mid-trimester Fetal Diagn Ther 14 1999 20 23