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1.
Ginekol Pol ; 85(3): 230-3, 2014 Mar.
Artículo en Polaco | MEDLINE | ID: mdl-24783437

RESUMEN

Chorioangioma (chorionic angioma) is the most common non-malignant placental tumor Taking into account its morphological structure, it can have significant influence on fetal condition and pregnancy depending on its size. In the presented case a substantial placental tumor was diagnosed and complications typical for chorioangioma, such as fetal hemodynamic disorders, polyhydramnios, gestational diabetes and premature labor were observed. The applied treatment led to normalization of the fetal and maternal condition and to prolongation of the pregnancy


Asunto(s)
Enfermedades Fetales/diagnóstico , Hemangioma/diagnóstico , Enfermedades Placentarias/diagnóstico , Polihidramnios/diagnóstico , Complicaciones Neoplásicas del Embarazo/diagnóstico , Adulto , Diabetes Gestacional/diagnóstico , Diabetes Gestacional/etiología , Femenino , Hemangioma/complicaciones , Hemangioma/patología , Hemangioma/terapia , Humanos , Trabajo de Parto Prematuro/etiología , Enfermedades Placentarias/patología , Enfermedades Placentarias/terapia , Polihidramnios/etiología , Embarazo , Complicaciones Neoplásicas del Embarazo/patología , Complicaciones Neoplásicas del Embarazo/terapia , Adulto Joven
3.
Ginekol Pol ; 81(8): 629-32, 2010 Aug.
Artículo en Polaco | MEDLINE | ID: mdl-20873127

RESUMEN

Thanatophoric dysplasia was first described in 1967 by Maroteaux. It is one of the most common lethal neonatal dwarfisms. Estimated incidence of thanatophoric dysplasia is 0.2-0.5 per 10,000 births. In the following report we have described a prenatally diagnosed case of recurrent thanatophoric dysplasia in the same patient.


Asunto(s)
Linaje , Segundo Trimestre del Embarazo/genética , Displasia Tanatofórica/diagnóstico por imagen , Displasia Tanatofórica/genética , Resultado Fatal , Femenino , Humanos , Embarazo , Ultrasonografía Prenatal
4.
Ginekol Pol ; 81(12): 940-3, 2010 Dec.
Artículo en Polaco | MEDLINE | ID: mdl-21395086

RESUMEN

Holoprosencephaly is a brain malformation caused by abnormal division of the forebrain into two separate hemispheres. Abnormal structures of the central nervous system often occur with other midline forebrain and face failures. In this report we present a case of a prenatal diagnosis of holoprosencephaly.


Asunto(s)
Holoprosencefalia/diagnóstico por imagen , Holoprosencefalia/embriología , Ultrasonografía Prenatal , Adulto , Resultado Fatal , Femenino , Humanos , Recién Nacido , Embarazo , Tercer Trimestre del Embarazo
5.
Ginekol Pol ; 80(10): 778-81, 2009 Oct.
Artículo en Polaco | MEDLINE | ID: mdl-19943544

RESUMEN

Smith-Lemli-Opitz syndrome (SLOS) is a hereditary, autosomal recessive abnormality of cholesterol metabolism, leading to malformations of multiple organs. It is probably one of the most frequent metabolic disorders but variable clinical presentation makes the diagnosis of the syndrome difficult. The authors of the following work present a case report of prenatal diagnosis of SLOS in fetus with malformations of multiple organs and negative family history.


Asunto(s)
Enfermedades Fetales/diagnóstico , Diagnóstico Prenatal/métodos , Síndrome de Smith-Lemli-Opitz/diagnóstico , Resultado Fatal , Femenino , Enfermedades Fetales/genética , Humanos , Recién Nacido , Embarazo , Síndrome de Smith-Lemli-Opitz/genética
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