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BMJ Case Rep ; 20132013 Dec 03.
Artículo en Inglés | MEDLINE | ID: mdl-24302663

RESUMEN

Werner's syndrome (WS) is a rare autosomal recessive disorder, characterised by skin changes prematurely during adolescence. An unusual case of WS was found in a 27-year-old pregnant woman who presented to the hospital with a history of uncontrolled hypertension at 32 weeks of gestation. All clinical features corresponding to WS (early aging of skin, hair loss, blurred vision and diabetes type 2) appeared to match with the prospective diagnosis, which was confirmed later with genetic testing. The pregnancy became complicated due to oligohydramnios and therefore a caesarean section was carried out in order to preserve the fetus. Despite all implemented efforts, the patient died intraoperative as a result of cardiac arrest and its complications. Successfully, the newborn survived and it was further investigated to exclude this condition.


Asunto(s)
Complicaciones del Embarazo/diagnóstico , Síndrome de Werner/diagnóstico , Adulto , Cesárea , Diagnóstico Diferencial , Resultado Fatal , Femenino , Humanos , Hallazgos Incidentales , Embarazo , Diagnóstico Prenatal
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