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Fetal Pediatr Pathol ; 42(1): 131-136, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-35414337

RESUMO

Background. Adams-Oliver syndrome is a congenital disease whose main findings are aplasia cutis congenita of the scalp and terminal transverse limb defects. The pathogenesis is unknown, but it is postulated that ischemic events in susceptible tissues cause the lesions in the embryonic period.Case report. We present a newborn with a severe phenotype of Adams-Oliver syndrome. The infant's mother had a SARS-CoV-2 infection in the first trimester of pregnancy. Prenatal ultrasound indicates a probable worsening of the disease after the first trimester.Conclusion. This study shows a previously unpublished severe AOS phenotype in a term newborn. There are some signs that the disease could have progressed beyond the first trimester, either spontaneously or by the inflammatory mechanisms of SARS-CoV-2.


Assuntos
COVID-19 , Displasia Ectodérmica , Deformidades Congênitas dos Membros , Humanos , SARS-CoV-2 , COVID-19/complicações , Displasia Ectodérmica/complicações , Deformidades Congênitas dos Membros/diagnóstico , Couro Cabeludo/anormalidades
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