article · Clinical Dysmorphology

Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature

Prince Makay
Jean‐Stéphane Gatot
Vincent Bours
Ines Sonet
Corinne Fasquelle
Prosper Lukusa-Tshilobo
Gerrye Mubungu
Patrick Fuanani
Benoît Charloteaux
Léonor Palmeira
Koenraad Devriendt
Aimée Mupuala
Esther Ekolo
Aimé Lumaka

2024Open accessUniversité de Kinshasa (UNIKIN)

Abstract

sponsorship: No Statement Available (VLIRUOShttp://dx.doi.org/10.13039/501100022083, National Institute for Mental Health (NIMH) of the National Institutes of Health (NIH)|R01HG012284, National Institute for Mental Health (NIMH) of the National Institutes of Health (NIH)|U01MH115483, Region of Wallonia|RWAL1710180, Flemish research council (VLIR))

Research topics

Hedgehog Signaling Pathway Studies
Congenital limb and hand anomalies
Genetic and rare skin diseases.

Sustainable Development Goals

2Zero Hunger

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DOI: 10.1097/mcd.0000000000000510

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