Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Banco de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
BMJ Case Rep ; 20172017 Feb 02.
Artículo en Inglés | MEDLINE | ID: mdl-28154155

RESUMEN

Congenital analbuminaemia is a rare autosomal recessive disorder that is characterised by a severe reduction or total absence of serum albumin. This condition has implications for therapeutics as a large proportion of commonly used drugs are plasma protein bound where albumin is the primary component of plasma protein. This is the first case report of pregnancy in a patient with congenital analbuminaemia in the medical literature. In the absence of drug dosage guidelines for patients with congenital analbuminaemia, a list of drugs which may be required for this patient during pregnancy, delivery and/or emergency situations were compiled by a multidisciplinary team. Our patient suffered from polyhydramnios during her pregnancy which was successfully managed with albumin transfusions and had a normal vaginal delivery with no complications in the intrapartum or postpartum period. The management and unique challenges of pregnancy in a patient with congenital analbuminaemia are discussed.


Asunto(s)
Anomalías Congénitas/diagnóstico , Polihidramnios/diagnóstico , Complicaciones del Embarazo/diagnóstico , Albúmina Sérica/deficiencia , Parto Obstétrico , Femenino , Humanos , Mutación , Polihidramnios/diagnóstico por imagen , Polihidramnios/tratamiento farmacológico , Embarazo , Albúmina Sérica/administración & dosificación , Albúmina Sérica/genética , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA