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[Discordant Down syndrome risk calculation with low maternal serum markers: About five cases of digynic triploidies]. / Risque de trisomie 21 discordant en cas de marqueurs sériques très bas : à propos de cinq cas de triploïdie digynique.
Roland, E; Voirin-Mathieu, E; Verchain, S; Odaert, H; Dreux, S; Renom, G.
Afiliação
  • Roland E; Laboratoire de dépistage périnatal, centre de biologie pathologie génétique, CHU, CS 70002, 59037 Lille cedex, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France.
  • Voirin-Mathieu E; Laboratoire de biochimie prénatale, hôpital Robert Debré, 48, boulevard Sérurier, 75935 Paris cedex 19, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France.
  • Verchain S; Laboratoire de biologie, centre hospitalier, 3, boulevard Besnier, CS 90006, 62022 Arras cedex, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France.
  • Odaert H; Laboratoire diagnovie-biogroup, 121, avenue Jean Jaurès, 59790 Ronchin, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France.
  • Dreux S; Laboratoire de biochimie prénatale, hôpital Robert Debré, 48, boulevard Sérurier, 75935 Paris cedex 19, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France.
  • Renom G; Laboratoire de dépistage périnatal, centre de biologie pathologie génétique, CHU, CS 70002, 59037 Lille cedex, France; ABA: Association des Biologistes Agréés pour le dépistage de la trisomie 21 fœtale, France. Electronic address: gilles.renom@chu-lille.fr.
Gynecol Obstet Fertil Senol ; 51(3): 172-175, 2023 03.
Article em Fr | MEDLINE | ID: mdl-36462714
ABSTRACT

OBJECTIVE:

We compare the risk of Down syndrome among five patients carrying a foetus with digynic triploidy and suggest a course of action for these particular serological profiles.

METHODS:

The concentrations of the different markers used are transformed into multiples of the median by using each of the three software types present on the French market which then determine the risk of Down syndrome.

RESULTS:

For comparable biochemical and ultrasound profiles, the risk of Down syndrome turns out to be vastly different depending on the type of software employed. The relevance of an immediate diagnostic procedure, of a cell free DNA test or of a basic ultrasound follow-up then arises, leading to a potentially variable care pathway for the patient.

CONCLUSIONS:

This study confirms that for this type of biochemical profile, the laboratory's advisory service is fundamental, that a control ultrasound is essential and that an invasive procedure must be used almost invariably due to the extremely substantial risk factors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Down Idioma: Fr Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Down Idioma: Fr Ano de publicação: 2023 Tipo de documento: Article