Secuencia de Potter, revisión de una enfermedad en el olvido
Date
Subject
Secuencia de Potter
oligohidramnios
agenesia renal
hipoplasia pulmonar
amnioinfusión
Potter sequence
oligohydramnios
renal agenesis
lung hipoplasia
amnioinfusion
oligohidramnios
agenesia renal
hipoplasia pulmonar
amnioinfusión
Potter sequence
oligohydramnios
renal agenesis
lung hipoplasia
amnioinfusion
Language:
Journal Title
Journal ISSN
Volume Title
Publisher
Intituto Tecnológico de Santo Domingo (INTEC)
Introducción:
la secuencia de Potter (SP) es un trastorno congénito se caracteriza por presentar oligohidramnios, agenesia renal e hipoplasia pulmonar que lleva a que los recién nacidos desarrollen dificultad respiratoria dentro de la primera hora del nacimiento.
Objetivo:
realizar una revisión exhaustiva sobre las actualizaciones del tema de Secuencia de Potter y nuevas intervenciones
Métodos:
se realizó una revisión de artículos en los buscadores PubMed, Ebsco, Google Académico, Scielo, Science Direct, entre otras, tanto en español e inglés. De la búsqueda fueron consultados 35 artículos.
Conclusión:
la SP es una enfermedad que se presenta en los fetos como consecuencia de una serie de eventos que ocurren por el oligohidramnios. Este se caracteriza por la facie de Potter, anomalías en las extremidades por compresión, y la hipoplasia pulmonar, siendo esta presentación clínica variable en cada paciente y a la cual se le añaden otras presentaciones infrecuentes. Si bien es cierto que, en la mayoría de los casos el pronóstico de esta enfermedad es desfavorable, se han investigado y llevado a cabo diversas intervenciones enfocadas en el aumento del líquido amniótico y la esperanza de vida de quienes padecen esta enfermedad.
Introduction: Potter's sequence (PS) is a congenital disorder characterized by oligohydramnios, renal agenesis, and pulmonary hypoplasia that leads to newborns developing respiratory distress within the first hour of birth. Objective: to carry out an exhaustive review of the updates of the Potter Sequence theme and new interventions Methods: a review of articles was carried out in PubMed, Ebsco, Google Scholar, Scielo, and Science Direct search engines, among others, both in Spanish and English. From the search, 35 articles were consulted. Conclusion: PS is a disease that occurs in fetuses as a consequence of a series of events that occur due to oligohydramnios. This is characterized by the Potter facie, anomalies in the extremities due to compression, and pulmonary hypoplasia, this clinical presentation being variable in each patient and to which other infrequent presentations are added. Although it is true that, in most cases, the prognosis of this disease is unfavorable, various interventions focused on increasing amniotic fluid have been investigated and carried out in order to increase the life expectancy of those who suffer from this disease.
Introduction: Potter's sequence (PS) is a congenital disorder characterized by oligohydramnios, renal agenesis, and pulmonary hypoplasia that leads to newborns developing respiratory distress within the first hour of birth. Objective: to carry out an exhaustive review of the updates of the Potter Sequence theme and new interventions Methods: a review of articles was carried out in PubMed, Ebsco, Google Scholar, Scielo, and Science Direct search engines, among others, both in Spanish and English. From the search, 35 articles were consulted. Conclusion: PS is a disease that occurs in fetuses as a consequence of a series of events that occur due to oligohydramnios. This is characterized by the Potter facie, anomalies in the extremities due to compression, and pulmonary hypoplasia, this clinical presentation being variable in each patient and to which other infrequent presentations are added. Although it is true that, in most cases, the prognosis of this disease is unfavorable, various interventions focused on increasing amniotic fluid have been investigated and carried out in order to increase the life expectancy of those who suffer from this disease.
Description
Type
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/publishedVersion
Source
Science and Health; Vol. 9 No. 1 (2025): Science and Health, january-march; 81-88
Ciencia y Salud; Vol. 9 Núm. 1 (2025): Ciencia y Salud, enero-marzo; 81-88
2613-8824
2613-8816
10.22206/cisa.2025.v9i1
Ciencia y Salud; Vol. 9 Núm. 1 (2025): Ciencia y Salud, enero-marzo; 81-88
2613-8824
2613-8816
10.22206/cisa.2025.v9i1