DOI: 10.1055/s-00057371

Journal of Fetal Medicine

Issue 03 · Volume 11 · September 2024 DOI: 10.1055/s-014-60456

Original Article

  • 145
    Dias, Zaneta; Elayedatt, Rinshi; Krishnan, Vivek:

    Placental Chorioangiomas: A Single Tertiary Center Experience

    Open Access Video available
  • 152
    Mahajan, Rahul; Elayedatt, Rinshi; Krishnan, Vivek:

    DiGeorge Syndrome: Prenatal Diagnosis and Outcome in a Tertiary Care Fetal Medicine Center

    Open Access

    • Editorial

  • 159
    Mukherjee, Kanchan; Mukherjee, B. Rishi:

    Reporting and Documentation of Obstetric Ultrasound Scans

    Open Access

    • SFM Practice Guidelines

  • 162
    Bhatt, Reema; Makam, Adinarayan:

    SFM Fetal Therapy Practice Guidelines: Fetoscopic Endoluminal Tracheal Occlusion

    Open Access
  • 167
    Dadhwal, Vatsla; Sahay, Neha; Sharma, K. Aparna:

    Standard Operating Procedures Ex Utero Intrapartum Therapy (EXIT)

    Open Access

    • Technology Showcase

  • 172
    Ghonge, Nitin P.:

    Agenesis of Corpus Callosum in a Fetus at 22 Weeks: Role of MRI Based Scoring and MR Tractography in Clinical Decision Making

    Open Access

    • Case Report

  • 175
    Roy, Prasanna; Dey, Shankar:

    A Case Report of Fetal Split Hand Foot Malformation Syndrome: A Rare Congenital Limb Anomaly

    Open Access
  • 179
    Paradkar, Priyanka Vishvanath; Redishetty, Saritha; Vavilala, Suseela:

    Spontaneous Rupture of Prenatally Detected Thoracic Neurenteric Cyst: Case Report and Review of Literature

    Open Access
  • 185
    Varshney, Alok; Kapoor, Aakriti; Kaur, Shina; Kapoor, Tushar; Kapoor, Aakaar; Kapoor, Apurva; Kapoor, Ravi:

    Fetal Ganglioneuroblastoma: A Rare Entity with Antenatal Diagnosis and Postnatal Follow Up

    Open Access

    • Case Series

  • 188
    Potdar, Omkar; Suresh, Indrani; Raja, Vijayalakshmi; Yadav, Sakshi:

    Diagnostic Dilemmas in Fetal Scalp Cystic Lesions: A Case Series

    Open Access

    • Brief Report

  • 193
    Gupta, Mansi; Nerakh, Gayatri:

    Clinical and Molecular Aspects of Craniofrontonasal Syndrome due to Contiguous Gene Deletion Involving AWAT2, EFNB1, EDA, OTUD6A, and PJA1 Genes

    Open Access