2q37 deletion syndrome in a Colombian patient with macrocephaly: a case report

BACKGROUND: 2q37 deletion syndrome is a rare autosomal dominant disorder caused by deletions in the 2q37 cytobands leading to developmental delay, intellectual disability, behavioral abnormalities and dysmorphic craniofacial features with more than 115 patients described worldwide. CASE PRESENTATION...

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Detalles Bibliográficos
Autores principales: Giraldo-Ocampo, Sebastian, Pachajoa, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531440/
https://www.ncbi.nlm.nih.gov/pubmed/36192675
http://dx.doi.org/10.1186/s12887-022-03620-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531440/
https://www.ncbi.nlm.nih.gov/pubmed/36192675
http://dx.doi.org/10.1186/s12887-022-03620-8

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