Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali

This case report details the first confirmed diagnosis of Trisomy 13 (Patau syndrome) in Mali using Fluorescence In Situ Hybridization (FISH). The male newborn presented with multiple congenital anomalies, including polydactyly and micrognathia. The diagnosis expands the understanding of Trisomy 13 in Africa, highlighting the importance of genetic testing in resource-limited settings.

Authors

Guida Landouré (ORCID: https://orcid.org/0000-0002-5921-7832)
Alassane Baneye Maīga (ORCID: https://orcid.org/0000-0002-7296-7785)
C O Sidibé
Oumar Samassékou (ORCID: https://orcid.org/0000-0003-1916-4534)
Oumou Traoré
Mahamadou Traoré
Cheick O. Guinto
Belco Maïga

Institutions

University of Bamako (ML)
Centre Hospitalier Universitaire de Tours (FR)
Université des Sciences, des Techniques et des Technologies de Bamako (ML)

Publication Details

Journal: Clinical Case Reports
Published: 2025-10-01
DOI: https://doi.org/10.1002/ccr3.71093
Primary Topic: Prenatal Screening and Diagnostics
Type: article
Field-Weighted Citation Impact: 0.00

Funders

Canadian Institutes of Health Research

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article

Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali

Guida Landouré, Alassane Baneye Maīga, C O Sidibé, Oumar Samassékou et al.

Oct 1, 2025

Clinical Case Reports

Prenatal Screening and Diagnostics

article

Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali

Guida Landouré, Alassane Baneye Maīga, C O Sidibé, Oumar Samassékou, Oumou Traoré, Mahamadou Traoré, Cheick O. Guinto, Belco Maïga

October 1, 2025article en

Abstract

This case report details the first confirmed diagnosis of Trisomy 13 (Patau syndrome) in Mali using Fluorescence In Situ Hybridization (FISH). The male newborn presented with multiple congenital anomalies, including polydactyly and micrognathia. The diagnosis expands the understanding of Trisomy 13 in Africa, highlighting the importance of genetic testing in resource-limited settings.

Clinical Case ReportsVol. 13(10)

University of Bamako (ML), Centre Hospitalier Universitaire de Tours (FR), Université des Sciences, des Techniques et des Technologies de Bamako (ML)

Canadian Institutes of Health Research

Openalex Percentile: Top 61%

Prenatal Screening and Diagnostics

DOI Open Access PDF OpenAlex

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Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali — Guida Landouré, Alassane Baneye Maīga, et al. · Clinical Case Reports (2025) | TGRS Research Map | TGRS