Congenital Toxoplasmosis in Tunisia: Prenatal and Neonatal Diagnosis and Postnatal Follow-up of 35 Cases

Yosr Boudaouara Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institute Pasteur of Tunis, Tunis, Tunisia;

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Karim Aoun Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institute Pasteur of Tunis, Tunis, Tunisia;
Department of Parasitology, Institute Pasteur of Tunis, Tunis, Tunisia

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Rania Maatoug Department of Parasitology, Institute Pasteur of Tunis, Tunis, Tunisia

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Olfa Souissi Department of Parasitology, Institute Pasteur of Tunis, Tunis, Tunisia

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Aïda Bouratbine Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institute Pasteur of Tunis, Tunis, Tunisia;
Department of Parasitology, Institute Pasteur of Tunis, Tunis, Tunisia

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Rym Ben Abdallah Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institute Pasteur of Tunis, Tunis, Tunisia;
Department of Parasitology, Institute Pasteur of Tunis, Tunis, Tunisia

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Congenital toxoplasmosis (CT) results from transplacental passage of Toxoplasma gondii to the fetus during acute maternal infection. Our study aims to report clinical and biological patterns of 35 cases of CT diagnosed at the department of the Parasitology of the Pasteur Institute of Tunis and to access the performance of prenatal and early postnatal diagnosis techniques. Serological screening of maternal infection was performed by Immunoglobulin (Ig) M and IgG detection and IgG avidity determination. Prenatal diagnosis was based on both Toxoplasma DNA detection in the amniotic fluid and monthly ultrasound examinations. polymerase chain reaction analysis on amniotic fluid, performed only in 15 cases, detected Toxoplasma’s DNA in five cases (33.3%). Ultrasound examination did not reveal any morphological abnormalities. Thirty newborns had serological criteria of Toxoplasma infection. Congenital toxoplasmosis diagnosis was confirmed in 23 cases (76.6%) by immunoblot. Among the 35 born-infants, five (14.3%) were symptomatic: three had chorioretinitis at the first clinical ocular examination, one had neurological symptoms (seizures) with positive parasite DNA in cerebral spinal fluid, and one had both ophthalmological and neurological damages— chorioretinitis and intracranial calcifications in the computed tomography scan. Thirty-four of 35 infected children were treated with pyrimethamine–sulfadiazine combination. Four (11.7%) of the treated infants showed abnormal hematological values because of the treatment side effect. Serological rebound was observed in seven infants. A screening program and a diagnostic algorithm in pregnant women should be implemented in Tunisia to improve the follow-up of seronegative ones and to prevent CT cases.

Author Notes

Address correspondence to Rym Ben Abdallah, Department of Parasitology, Institute Pasteur of Tunis, 13 Place Pasteur, BP 74, Tunis 1002, Tunisia. E-mail: ismail_rym@yahoo.fr

Authors’ addresses: Yosr Boudaouara, Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia, E-mail: boud.yosr@gmail.com. Karim Aoun, Lab of Parasitology, Department of Parasitology, Institut Pasteur de Tunis, Tunis, Tunisia, E-mail: karim.aoun@pasteur.rns.tn. Rania Maatoug, Olfa Souissi, and Aïda Bouratbine, Department of Parasitology, Institut Pasteur de Tunis, Tunis, Tunisia, E-mails: raniamaatoug@gmail.com, souissiolfa75@yahoo.fr, and aida.bouratbine@pasteur.rns.tn. Rym Ben Abdallah, Department of Parasitology, Institut Pasteur de Tunis, Tunis, Tunisia, and Research Laboratory Medical Parasitology, Biotechnology and Biomolecule LR11IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia, E-mail: ismail_rym@yahoo.fr.

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