Discussion on: A Novel Homozygous HERC2 c.4660C>T (p. Arg1554Ter) Variant in an Infant with Severe Neurodevelopmental Disorder and Diffuse Osteopenia: A Case Report

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Article Title

A Novel Homozygous HERC2 c.4660C>T (p. Arg1554Ter) Variant in an Infant with Severe Neurodevelopmental Disorder and Diffuse Osteopenia: A Case Report

Authored by

Abdillahi Moustapha
Department of Pediatrics, Mohamed V Military Training Hospital, Rabat, Morocco and Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco.

Laarage Azzeddin
Department of Pediatrics, Mohamed V Military Training Hospital, Rabat, Morocco and Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco.

A. Radi
Department of Pediatrics, Mohamed V Military Training Hospital, Rabat, Morocco and Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco.

R. Abikassem
Department of Pediatrics, Mohamed V Military Training Hospital, Rabat, Morocco and Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco.

DOI or Article Link

https://doi.org/10.9734/ajpr/2026/v16i10582

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