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1.859  Articles
1 of 187 pages  |  10  records  |  more records»

Diagnóstico prenatal ecográfico del Síndrome Klippel-Trenaunay-Weber: a propósito de un caso / Prenatal sonographic diagnosis of Klippel-Trenaunay-Weber syndrome: a case reportDiagnóstico prenatal ecográfico del Síndrome Klippel-Trenaunay-Weber: a propósito de un caso / Prenatal sonographic diagnosis of Klippel-Trenaunay-Weber syndrome: a case reportEl estudio del feto utilizando ultrasonido en tiempo real es uno de los avances tecnológicos más importantes de los últimos tiempos, permitiendo obtener información acerca de su integridad anatómica y funcional, así como establecer el diagnóstico de defectos congénitos en las etapas tempranas del embarazo. El Síndrome Klippel-Trenaunay-Weber fue originalmente reportado por Maurice Klippel y P. Trenaunay en 1900, el hallazgo clínico más frecuente es el angioma plano o nevus flammeus. Se presenta un caso de una gestante de 18 años, primigesta, con antecedente de salud previo, que acude a la consulta por presentar Hb AS. El estudio ecográfico realizado a las 22 semanas de gestación reveló marcada hipertrofia del miembro inferior izquierdo fetal asociado a hemangioma cavernoso gigante que afectaba pelvis, nalgas y genitales. Tales hallazgos guiaron al diagnóstico de Síndrome Klippel-Trenaunay-Weber. Esta entidad clínica es considerada una rareza, siendo su diagnóstico prenatal ecográfico poco conocido por lo que se presenta el caso.Palabras clave: Síndrome de Klippel-Trenaunay-Weber, ULTRASONOGRAFÍA PRENATAL.ABSTRACTThe study of the fetus using the ultrasound in real time is one of the most important technological advances of recent days; which allow collecting information about anatomic and functional integrity as well as establishing the diagnosis of congenital malformations in early stages of pregnancy. Klippel-Trenaunay-Weber syndrome was first reported by Maurice Klippel and P. Trenaunay in 1900, the most frequent clinical finding is the flat angioma or flammeus nevus. An 18 years old primigravida having health records attended to the office presenting HbAS. The sonographic study carried out at 22 weeks of pregnancy revealed a marked hypertrophy of the lower fetal limb associated with giant cavernous angioma affecting the pelvis, buttocks and genitals. Such findings guided to the diagnosis of Klippel-Trenaunay-Weber syndrome. This is a rare clinical entity and its antenatal diagnosis is little- known, thus the case is presented.Key words: Klippel-Trenaunay-Weber syndrome, PRENATAL ULTRASONOGRAPHY.

ABSTRACTThe study of the fetus using the ultrasound in real time is one of the most important technological advances of recent days; which allow collecting information about anatomic and functional integrity as well as establishing the diagnosis of congen... see more

IntroductionCongenital malformations are the main cause of miscarriage, perinatal mortality and disability among children. According to Polish Registry of Congenital Malformations for 2005-2006 congenital disorders affect 2.0-4.0% of newborns. Heart defec... see more

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Objective: To report a rare case of hydranencephaly that was diagnosed during prenatal period. We also provided further review of differential diagnosis and management performed in Ende District General Hospital, based on appropriate literatures and guide... see more

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Background:There is scanty data on the pattern of childhoodurogenital malformations in many resource-poorcountries, including Nigeria.Objective:To describe the pattern of occurrence of majorurogenital malformations in children presenting in atertiary heal... see more

ltrasound parameters during pregnancy and the growth of children aged 2 – 3 years.Methods: This was an analytic observational study with a longitudinal approach using data from the first 1,000 days of life. Study conducted at the Faculty of Medicine, Dipo... see more

Abstract (English)Objective: To report a rare case of thanatophoric skeletal dysplasia type 2 that we diagnosed during prenatal period; and to provide further review of dilemmas in diagnostic methods and management, based on appropriate literatures and gu... see more

Objective : To perform chromosomal microarray when similar case was found.Methods: Case reportCase : G1P0A0, 20 years-old, 23-24 weeks gestation, normal BMI, was diagnosed by ultrasonography with multiple congenital anomaly consisted by  meningoencep... see more

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