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No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.

Autor: Ibrahim I; School of Health Studies, Elborn College Western University London Ontario Canada., Scriver T; Division of Medical Genetics, Department of Pediatrics, Royal University Hospital University of Saskatchewan Saskatoon Saskatchewan Canada., Basalom SA; Division of Medical Genetics, Department of Pediatrics, Royal University Hospital University of Saskatchewan Saskatoon Saskatchewan Canada.

Publikováno v: Clinical case reports [Clin Case Rep] 2023 May 10; Vol. 11 (5), pp. e7332. Date of Electronic Publication: 2023 May 10 (Print Publication: 2023).