Hydrops fetalis is Latin for edema of the fetus. Ballantyne first described hydrops fetalis in , although this condition had been recognized. Hydrops fetalis is excessive extravasation of fluid into the third space in a fetus which could be due to heart failure, volume overload, decreased oncotic pressure. Hydrops fetalis is a serious condition which indicates poor prognosis for the affected fetus. Although the incidence of isoimmune hydrops fetalis.

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Non-immune hydrops can also be unrelated to anemia, for example bidrops a fetal tumor or congenital cystic adenomatoid malformation increases the demand for blood flow.

Management outcome and follow-up of fetal tachycardia. Antenatal diagnosis Because of the risks for the fetus and for the mother, prenatal diagnosis for Hb Bart’s hideops be offered. Sonographic evaluation of nuchal edema — a finding associated with a variety of fetal abnormalities — was first described in the axial plane in the second trimester.

An additional 20 or more reports of imprecisely defined chromosomal or genetic syndromes identify hydrops as an incidental finding. Hydrops fetalis is a condition in the fetus characterized by an accumulation of fluid, or edemain at least two fetal compartments.

HbA2 levels were higher than 3. Fetais description Edema, signs of heart failure and profound intra-uterine anemia are the presenting features in the fetus. Hydrops fetalis can be diagnosed and monitored by ultrasound scans. Retrieved from ” https: Hydrops fetalis caused by alpha-thalassemia: The disease occurs predominantly in Southeast Asia.


Analisis kromosom janin diindikasikan pada semua kasus hidrops. Fetalie 50 hidrope the more common errors are listed below. Early therapeutic termination of at-risk pregnancies is usually recommended due to the severity of the syndrome and the risk of potentially serious maternal complications during pregnancy.

In utero exchange transfusion in homozygous alpha-thalassaemia: Incidence of alpha-thalassemia in Turkey.

Hydrops fetalis | Radiology Reference Article |

Detailed information Article for general public Svenska Hemoglobin electrophoresis and HbA2 levels are often used as part of the laboratory investigations to diagnose thalassemia carriers. Cardiac Disease and Critical Care Medicine”. Vertically transmitted infection Neonatal infection Congenital rubella syndrome Neonatal herpes simplex Mycoplasma hominis infection Ureaplasma urealyticum infection Omphalitis Neonatal sepsis Group B streptococcal infection Neonatal conjunctivitis.

The main differential diagnosis is hydrops fetalis see this term without alpha-thalassemia, which is a common non-specific sign of numerous fetal or maternal disorders. Prenatal management of congenital cystic adenomatoid malformation of the lung. J Am Soc Echocardiogr. From Wikipedia, the free encyclopedia. Alpha thalassemia major–new mutations, intrauterine management, and outcomes.

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Hb Bart’s hydrops fetalis is the most severe form of alpha-thalassemia see this term and is almost always lethal. Previous page of related Sponsored Products. Intrauterine hypoxia Infant respiratory distress syndrome Transient tachypnea of the newborn Meconium aspiration syndrome pleural disease Pneumothorax Pneumomediastinum Wilson—Mikity syndrome Bronchopulmonary dysplasia.

Fetal and placental edema accompanied by serous effusions first was described generations ago. Primary congenital pulmonary lymphangiectasis reflects hidrpps abnormality of lymphatic development. She died shortly after birth despite supportive treatment. No gene deletions were detected in the mother, although her hematological parameters were consistent with thalassemia. National Center for Biotechnology InformationU.


Hydrops fetalis – Wikipedia

Respiratory Intrauterine hypoxia Infant respiratory distress syndrome Transient tachypnea of the newborn Meconium aspiration syndrome pleural disease Pneumothorax Pneumomediastinum Wilson—Mikity syndrome Bronchopulmonary dysplasia. This results in a progressive severe anemia and tissue hypoxia.

Red cell indices of both parents and the sister showed microcytosis and eftalis despite the lack of iron deficiency. Etiology Bart’s hydrops fetalis is caused by deletion or inactivation of all four alpha-globin alleles leading to a severe deficiency in alpha-globin chains of Hb, and to the production of gamma-4 tetramers Hb Bart.

In-utero haematopoietic stem cell transplantation: Journal List Turk J Haematol v. Exact incidence in other regions is not nidrops. Diagnostic methods The disease is usually diagnosed on ultrasound at 22 to 28 weeks gestation and can be suspected in at-risk pregnancies at 13 to 14 weeks gestation when increased nuchal or placental thickness, and increased cardiothoracic ratio are found.

The most ideal approach would be in utero stem cell transplantation before fetal immunological maturation [ 10 ].

The non-immune form of hydrops fetalis has many causes including: No gene deletions were detected in the mother. Transfusi intrauterin untuk anemia b. D ICD –