American Journal of Perinatology Reports
Ausgabe 03 · Juli 2024
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Case Report
e193
Soufan, Maya; Soufan, Haya; Chaudhari, Kushagra; Klarr, Judith:
A Case of Congenital Myasthenia Gravis due to ChAT Gene Mutation in a Term Neonate: A Case Report
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e202
Berger, Dana Senderoff; Robinson, Andre; Chervenak, Judith; Thomas, Kristen; Srinivasan, Ranjini; Sharma, Geeta; Roman, Ashley S.; Penfield, Christina A.; Limaye, Meghana:
A Case of Vein of Galen Aneurysmal Malformation Diagnosed Prenatally in a Monochorionic-Diamniotic Twin Pregnancy
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e205
Rodriguez, Stephanie; Marty, Daisy; Folga, Barbara; Alrahmani, Layan:
Congenital Umbilical Cord Hernia: Prenatal and Postnatal Management
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e224
Reguero Cadilla, Laura; Villafuerte Santana, Carlos; Centazzo, Nicolle; Faustin, Daniel:
Rare Case of Twin Reversed Arterial Perfusion
Acardius Acephalus
Subtype Seen in a Community-Based Hospital
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e228
Rodriguez, Stephanie; DeChristopher, Phillip J.; Krum, Kristen; Lal, Ann:
Anti-D Alloimmunization in Index Pregnancy after Appropriate Rho(D) Immune Globulin Injection in Two Obese Rh-Negative Patients
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e231
Jerbi, Bilel; Chourou, Hajer; Ben Aziza, Rim; Belhadj Ammar, Wafa; Kacem, Samia; Achour, Radhouane:
Early Challenges: A Case Report of a Premature Baby with Down Syndrome and Uterine Rupture
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e235
Liang, Alvina; Idowu, Mary Boluwatife; Eskind, Steven Joseph; Patel, Soha S.:
Necrotizing Fasciitis Post-Cesarean Section Leading to Transabdominal Hysterectomy
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e239
Sagaser, Anna E.; Reeves, Ashley; Arnautovic, Tamara; Sanchez-Esteban, Juan:
Distinction between Pneumothorax and Pneumomediastinum Using Point of Care Ultrasound (POCUS): Role of Still Lung Point
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Original Article
e197
Zohar, Noa; Katz-Leurer, Michal; Zuk, Luba; Israeli-Mendlovic, Hadas:
Preterm Infant's Heart Rate Variability Near Birth Predicts Autonomic Symptoms at Age 3 to 5 Years
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e208
Xie, Juan; Ling, Yu; Zhou, Xiaoyu:
Predeposit Autologous Blood Donation in Rh(D)-Negative Pregnant Women: A Single-Center Study
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Case Reports
e215
Lu, Yurong; Tian, Yijia; Liu, Jinxiu; Wang, Yifan; Wang, Xietong:
A
De novo
Mutation in the
COL1A1
Gene Leading to Severe Osteogenesis Imperfecta: Case Report and Review of the Literature
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