Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotype

Statement of ethics

The research was conducted ethically in accordance with the World Medical Association Declaration of Helsinki. Patient’s parents have given their written informed consent to publish their case. Whole exome sequencing including was performed on the patient upon receiving informed consent from patient’s parents. Our institution does not require ethical approval for reporting individual cases.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images.

Conflict of Interest Statement

The authors declare no competing interests.

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