Introduction |
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1 | (3) |
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Nuchal translucency and chromosomal defects |
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3 | (64) |
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Calculation of risk for chromosomal defects |
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8 | (6) |
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Nuchal translucency thickness |
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14 | (15) |
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Increased nuchal translucency and other chromosomal defects |
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29 | (2) |
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Crown-rump length in chromosomally abnormal fetuses |
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31 | (2) |
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Fetal heart rate in chromosomally abnormal fetuses |
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33 | (3) |
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Doppler ultrasound findings in chromosomally abnormal fetuses |
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36 | (2) |
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Nuchal translucency and maternal serum biochemistry |
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38 | (3) |
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Nuchal translucency followed by second-trimester biochemistry |
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41 | (2) |
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Nuchal translucency followed by second- trimester ultrasonography |
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43 | (3) |
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Non-invasive diagnosis using fetal cells from maternal blood |
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46 | (4) |
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Invasive diagnosis of chromosomal defects |
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50 | (17) |
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Increased nuchal translucency with normal karyotype |
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67 | (28) |
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68 | (1) |
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The Fetal Medicine Foundation Project |
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68 | (3) |
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Fetal defects presenting with increased nuchal translucency thickness |
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71 | (1) |
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Consequences of increased nuchal translucency |
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71 | (2) |
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Conditions associated with increased nuchal translucency |
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73 | (1) |
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73 | (3) |
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76 | (1) |
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77 | (1) |
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77 | (1) |
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78 | (1) |
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Asphyxiating thoracic dystrophy |
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78 | (1) |
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Beckwith-Wiedemann syndrome |
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78 | (1) |
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Blomstrand osteochondrodysplasia |
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79 | (1) |
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79 | (1) |
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80 | (1) |
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Ectrodactyly-ectodermal dysplasia-cleft palate (EEC) syndrome |
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80 | (1) |
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Fetal akinesia deformation sequence (FADS) |
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81 | (1) |
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82 | (1) |
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82 | (1) |
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82 | (1) |
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83 | (1) |
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84 | (1) |
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84 | (1) |
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84 | (1) |
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85 | (1) |
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Osteogenesis imperfecta type II |
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85 | (1) |
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86 | (1) |
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86 | (1) |
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Short-rib polydactyly syndrome |
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86 | (1) |
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Smith-Lemli-Opitz syndrome |
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87 | (1) |
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Spinal muscular atrophy type 1 (Werdnig-Hoffmann disease) |
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87 | (1) |
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87 | (1) |
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Trigonocephaly `C' syndrome |
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88 | (1) |
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88 | (1) |
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88 | (7) |
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Pathophysiology of increased nuchal translucency |
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95 | (20) |
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Constantin von Kaisenberg |
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95 | (8) |
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Venous congestion in the head and neck |
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103 | (1) |
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Alteration in the extracellular matrix |
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104 | (4) |
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Lymphatic vessel hypoplasia |
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108 | (2) |
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Anemia and hypoproteinemia |
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110 | (1) |
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110 | (5) |
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Diagnosis of fetal abnormalities at the 11-14-week scan |
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115 | (34) |
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Normal first-trimester ultrasound findings |
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115 | (8) |
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Abnormal ultrasound findings |
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123 | (1) |
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Central nervous system defects |
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123 | (8) |
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131 | (3) |
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134 | (3) |
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137 | (4) |
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141 | (8) |
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149 | (38) |
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Types of multiple pregnancy |
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149 | (1) |
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Incidence and epidemiology |
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149 | (1) |
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Zygosity and chorionicity |
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150 | (3) |
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Miscarriage and perinatal mortality |
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153 | (1) |
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154 | (1) |
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155 | (3) |
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Twin-to-twin transfusion syndrome |
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158 | (4) |
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162 | (2) |
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Death of one fetus in twin pregnancy |
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164 | (1) |
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Structural defects in multiple pregnancy |
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165 | (3) |
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Chromosomal defects in multiple pregnancy |
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168 | (6) |
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Prenatal determination of chorionicity |
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174 | (1) |
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Multifetal pregnancy and embryo reduction |
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175 | (12) |
Index |
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187 | |