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Intro; Foreword; Preface; Acknowledgements; Contents; Abbreviations; About the Author; 1: Neurosonoanatomy; 1.1 Echopattern of Intracranial Structures; 1.2 Sections of Basic Examination; 1.2.1 11-14 Weeks; Axial Transventricular Section; Midsagittal Section; Axial Transthalamopeduncular Section; Axial Transcerebellar Section; 1.2.2 18-22 Weeks; Axial Transventricular Section; Axial Transthalamic Section; Axial Transcerebellar Section; Coronal Transfrontal Section; Coronal Transcaudate Section; Coronal Transthalamic Section; Coronal Transcerebellar Section; Midsagittal Section
The Parasagittal Sections1.3 Sulcation and Gyration; 1.3.1 Classification of Sulci; Medial Hemispherical Group; Convexity Group; Inferior Group; Lateral Fissure; 1.3.2 Ultrasound Appearance and Evolution of Sulci and Lateral Fissure; Sulci; The Lateral Fissure; Suggested Reading; 2: Anomalies of Corpus Callosum and Septum Pellucidum; 2.1 Complete Agenesis of Corpus Callosum; 2.1.1 Indirect Signs in the Transventricular Axial Section; 2.1.2 Indirect Signs on Transcaudate Coronal Section; 2.1.3 Indirect Signs on the Midsagittal Section
2.1.4 Direct Sign on Midsagittal, Transcaudate and Transthalamic Coronal Sections2.1.5 Associated Intracranial Findings; 2.1.6 Associated Extracranial Findings; 2.1.7 Differential Diagnosis; 2.2 Partial Agenesis of Corpus Callosum; 2.2.1 Indirect Signs on Axial Sections; 2.2.2 Direct Signs on Midsagittal Section; 2.3 Other Callosal Abnormalities; 2.4 Septal Agenesis; Suggested Reading; 3: Anomalies of Ventral Induction: Holoprosencephaly; 3.1 Ultrasound Findings of HPE; 3.1.1 Alobar Holoprosencephaly; Differential Diagnosis; 3.1.2 Semilobar Holoprosencephaly
3.1.3 Lobar HoloprosencephalyDifferential Diagnosis; 3.1.4 Middle Hemispheric Variant; 3.1.5 Common Findings in All Types of HPE; 3.1.6 Midline Facial Defects in HPE; 3.1.7 Associated Anomalies; Suggested Reading; 4: Malformations of Cortical Development; 4.1 Disorders of Neuronal Proliferation; 4.1.1 Microcephaly; 4.1.2 Macrocephaly; 4.2 Disorders of Neuronal Migration; 4.2.1 Classical Lissencephaly; 4.2.2 Cobblestone Complex; 4.2.3 Neuronal Heterotopia; 4.2.4 Hemimegalencephaly; 4.3 Disorders of Neuronal Organisation; 4.3.1 Tuberous Sclerosis; 4.3.2 Schizencephaly
4.3.3 PolymicrogyriaSuggested Reading; 5: Anomalies of the Cerebellum; 5.1 Mega Cisterna Magna; 5.2 Blake's Pouch Cyst; 5.3 Vermian Hypoplasia; 5.4 Dandy-Walker Malformation; 5.5 Cerebellar Hypoplasia; 5.6 Rhombencephalosynapsis; 5.7 Joubert Syndrome and Related Cerebellar Disorders; Suggested Reading; 6: Anomalies of Dorsal Induction: Neural Tube Defects; 6.1 Anencephaly; 6.2 Iniencephaly; 6.3 Cephalocele; 6.3.1 Occipital Cephalocele; 6.3.2 Frontal Cephalocele; 6.3.3 Parietal Cephalocele; 6.3.4 Atretic Cephalocele; 6.4 Sonoanatomy of the Normal Spine; 6.4.1 Sagittal Section
The Parasagittal Sections1.3 Sulcation and Gyration; 1.3.1 Classification of Sulci; Medial Hemispherical Group; Convexity Group; Inferior Group; Lateral Fissure; 1.3.2 Ultrasound Appearance and Evolution of Sulci and Lateral Fissure; Sulci; The Lateral Fissure; Suggested Reading; 2: Anomalies of Corpus Callosum and Septum Pellucidum; 2.1 Complete Agenesis of Corpus Callosum; 2.1.1 Indirect Signs in the Transventricular Axial Section; 2.1.2 Indirect Signs on Transcaudate Coronal Section; 2.1.3 Indirect Signs on the Midsagittal Section
2.1.4 Direct Sign on Midsagittal, Transcaudate and Transthalamic Coronal Sections2.1.5 Associated Intracranial Findings; 2.1.6 Associated Extracranial Findings; 2.1.7 Differential Diagnosis; 2.2 Partial Agenesis of Corpus Callosum; 2.2.1 Indirect Signs on Axial Sections; 2.2.2 Direct Signs on Midsagittal Section; 2.3 Other Callosal Abnormalities; 2.4 Septal Agenesis; Suggested Reading; 3: Anomalies of Ventral Induction: Holoprosencephaly; 3.1 Ultrasound Findings of HPE; 3.1.1 Alobar Holoprosencephaly; Differential Diagnosis; 3.1.2 Semilobar Holoprosencephaly
3.1.3 Lobar HoloprosencephalyDifferential Diagnosis; 3.1.4 Middle Hemispheric Variant; 3.1.5 Common Findings in All Types of HPE; 3.1.6 Midline Facial Defects in HPE; 3.1.7 Associated Anomalies; Suggested Reading; 4: Malformations of Cortical Development; 4.1 Disorders of Neuronal Proliferation; 4.1.1 Microcephaly; 4.1.2 Macrocephaly; 4.2 Disorders of Neuronal Migration; 4.2.1 Classical Lissencephaly; 4.2.2 Cobblestone Complex; 4.2.3 Neuronal Heterotopia; 4.2.4 Hemimegalencephaly; 4.3 Disorders of Neuronal Organisation; 4.3.1 Tuberous Sclerosis; 4.3.2 Schizencephaly
4.3.3 PolymicrogyriaSuggested Reading; 5: Anomalies of the Cerebellum; 5.1 Mega Cisterna Magna; 5.2 Blake's Pouch Cyst; 5.3 Vermian Hypoplasia; 5.4 Dandy-Walker Malformation; 5.5 Cerebellar Hypoplasia; 5.6 Rhombencephalosynapsis; 5.7 Joubert Syndrome and Related Cerebellar Disorders; Suggested Reading; 6: Anomalies of Dorsal Induction: Neural Tube Defects; 6.1 Anencephaly; 6.2 Iniencephaly; 6.3 Cephalocele; 6.3.1 Occipital Cephalocele; 6.3.2 Frontal Cephalocele; 6.3.3 Parietal Cephalocele; 6.3.4 Atretic Cephalocele; 6.4 Sonoanatomy of the Normal Spine; 6.4.1 Sagittal Section