HIDROPESIA FETAL NO INMUNE PDF

Cytogenetic results, the evolution of the pregnancies, ultrasonographic images and pathologic studies were reviewed. Chromosome analysis were performed in 25 cases: 18 in amniotic fluid, 9 in chorionic villi and 2 in blood of the newborn. In one of these, the karyotype was normal, male; in the other, the cell culture was unsuccessful. In other cases with normal chromosomes, the pathologic study of the fetus or stillborn showed congenital malformations that could explain the development of hydrops. The proposed protocol fluxogram should facilitate the etiologic diagnosis, thus allowing genetic counseling and prevention of recurrence.

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Informe de un caso Anuncio www. Background: Hydrops fetalis is a clinical condition characterized by an abnormal fluid accumulation in soft tissues and in some serous cavities of the fetus. It is important to know beforehand if this condition is present in order to establish the most probable origin and to be prepared to administer optimal reanimation management of the neonate at birth.

The care given to a newborn with hydrops fetalis is always a challenge for the neonatologist. Case report. We present the case of a pregnant, nonisoimmunized patient with RhO negative blood type. Delivery was accomplished with Cesarean section where a female neonate of 32 weeks gestation was delivered.

Non-immune hydrops fetalis was present. We present recommendations for optimal diagnosis and therapy. Informe de un caso. Figura 1. Figura 2. Figura 3. Ecocardiograma en modo B en toma subcostal eje corto a nivel de grandes vasos, donde se observa la continuidad entre la arteria pulmonar y aorta descendente por el conducto arterioso permeable. Este manejo a pesar de ser controversial, fue aplicado con las precauciones recomendadas. Cuadro 1. Autor de correspondencia: Herminia Uscanga Carrasco.

Delivery room management. Pathophysiology and management of the newborn. Philadelphia: Lippincott, Williams and Wilkins; Perinatol Reprod Hum ; Trainor B, Tumban R.

The emerging pattern of hidrops fetalis- incidence, aetiology and management. Ulster Med J ; Perinat Ginecol Obstet ; Aetiology, diagnosis and treatment of hydrops fetalis. Curr Pediatr Rev ; An Facul Med ; Rev Chil Pediatr ; Mucopolysaccharidosis type VII as a cause of recurrent nonimmune hydrops fetalis. J Perinat Med ; Textbook of neonatal resuscitation. Arch Argent Pediatr ; Hidropesia fetal no inmunitaria: enfoque multidisciplinario.

Recurrent non-immune fetal hydrops: A Case report. Ann Acad Med ; Hidrops fetalis: reporte de 8 casos. Universidad de Carabobo; ; Reporte de un caso.

Rev Mex Pediatr ; Hydrops fetalis secondary to parvovirus B19 infections. J Am Board Fam Pract ; Fetal Diamond-Blackfan anemia associated with hidrops fetalis.

Am J Perinatol ; Rev Obstet Ginecol Venez ; Dos casos de hidrops fetalis no inmune.

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Hidropesía fetal

Informe de un caso Anuncio www. Background: Hydrops fetalis is a clinical condition characterized by an abnormal fluid accumulation in soft tissues and in some serous cavities of the fetus. It is important to know beforehand if this condition is present in order to establish the most probable origin and to be prepared to administer optimal reanimation management of the neonate at birth. The care given to a newborn with hydrops fetalis is always a challenge for the neonatologist.

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Hidropesía fetal. A propósito de un caso

Sazil Participation is free and the site has a strict confidentiality policy. Mirror syndrome may represent a form of preeclampsia, and is characterized by edema in approximately 90 percent, hypertension in 60 percent, and proteinuria in 40 percent of cases. Tiene una incidencia entre 1: However, many of these reports predate routine sonography and limited information is available on contemporary incidence of NIHF in a prenatal population. Peer comments on this answer tetal responses from the answerer. In one retrospective series, preterm birth prior to 34 weeks was a poor prognostic factor.

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