Chromosome 15q BP4–BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment

The 15q13.3 microdeletion (microdel15q13.3) syndrome (OMIM 612001) has been reported in healthy subjects as well as in individuals with a wide spectrum of clinical manifestations ranging from mild to severe neurological disorders, including developmental delay/intellectual disability, autism spectru...

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Detalles Bibliográficos
Autores principales: Pavone, Piero, Pappalardo, Xena Giada, Ohazuruike, Ugochi Ngaobiri Nelly, Striano, Pasquale, Parisi, Pasquale, Corsello, Giovanni, Marino, Simona Domenica, Ruggieri, Martino, Parano, Enrico, Falsaperla, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903043/
https://www.ncbi.nlm.nih.gov/pubmed/33659201
http://dx.doi.org/10.14581/jer.20014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903043/
https://www.ncbi.nlm.nih.gov/pubmed/33659201
http://dx.doi.org/10.14581/jer.20014

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