Hydrops fetalis is a well known condition with an extensive list of differential diagnoses. The etiology is divided into immunerelated and nonimmune-related types, and currently almost 90% of cases are associated with the latter category [1]. Among the various nonimmune-related causes, one of the most common are cardiac aberrations [2]. Prenatal ultrasound serves as the initial diagnostic tool ...

Hydrops fetalis is rarely caused by congenital dyserythropoietic anemia (CDA). We report a patient with hydrops fetalis as a result of severe anemia. This patient needed intrauterine transfusions from 21 weeks of gestation until birth. The hematologic study showed an atypical CDA (hydrops fetalis-associated CDA) characterized by features resembling CDA type II, but negative acidified serum lysi...

Introduction. Primary congenital lymphedema is a rare disorder associated with insufficient development of lymphatic vessels. Usually most patients present with lower extremity edema seen sonographically. Rarely primary congenital lymphedema may be associated with severe lymphatic dysfunction resulting in hydrops fetalis. Case. A 27-year-old primigravida with a family history of leg swelling th...

Teratomas are one of the most frequent tumors in the pediatric population. They occur anywhere along the midline of the body, following the course of the embryonic germ cell ridge. In the mediastinal location, they exert space occupying effects, leading to a myriad of complications, including non-immune hydrops fetalis. We describe a fatal case of an immature thymic teratoma in a neonate presen...

A = 5'GCGATCTGGGCTCTGTGTTCT-3' complications, such as hydramnios, preeclampsia, antepartum or postpartum hemorrhage, and difficult vaginal delivery? There is also considerable emotional strain for the mothers and their family members. We use polymerase chain reaction (PCR) and prenatal diagnosis from chorionic villi biopsy samples to identify couples at risk of conceiving fetuses afflicted with...

Hydrops fetalis is defined by the accumulation of fluids in serous membranes (pleurisy, ascites, pericarditis...), it a rare condition; its etiologies are divided into immunological and non-immunological. Supraventricular tachycardia remains known cause, non-immunological, but difficult to manage.
 In this article we report case newborn with hydrops secondary supraventricular tachycardia, ...

Background Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane. The disorder is commonly inherited in an autosomal dominant fashion and leads to a mild to moderate anemia. The autosomal recessive form of hereditary spherocytosis is rarely reported in association with fetal anemia and hydrops fetalis. Ca...

We studied a kindred in which four third-trimester fetal losses occurred, associated with severe Coombs-negative hemolytic anemia and hydrops fetalis. Postmortem examination of two infants revealed extensive extramedullary erythropoiesis. Studies of erythrocytes and erythrocyte membranes from the parents revealed abnormal erythrocyte membrane mechanical stability as well as structural and funct...

We studied a kindred in which four third-trimester fetal losses occurred, associated with severe Coombs-negative hemolytic anemia and hydrops fetalis. Postmortem examination of two infants revealed extensive extramedullary erythropoiesis. Studies of erythrocytes and erythrocyte membranes from the parents revealed abnormal erythrocyte membrane mechanical stability as well as structural and funct...