Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment-Reference-Cited by-同舟云学术

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

Published:2020-12-31 Issue:2 Volume:10 Page:84-91
ISSN:2233-6249
Container-title:Journal of Epilepsy Research
language:en
Short-container-title:J Epilepsy Res

Author:

Pavone Piero,Pappalardo Xena Giada,Nelly Ohazuruike Ugochi Ngaobiri,Striano Pasquale,Parisi Pasquale,Corsello Giovanni,Marino Simona Domenica,Ruggieri Martino,Parano Enrico,Falsaperla Raffaele

Publisher

Korean Epilepsy Society

Subject

General Medicine

Link

http://j-epilepsy.org/upload/jer-20014.pdf

Reference36 articles.

1. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

2. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

3. Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy

4. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

5. A de novo nonsense mutation in ZBTB18 plus a de novo 15q13.3 microdeletion in a 6‐year‐old female

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1. Pitt Hopkins syndrome – TCF4 gene deletion causing severe psychomotor delay;Human Gene;2024-09

2. Heterozygous Deletion of Chromosome 15q13.3 in a Boy with Developmental Regression, Global Developmental Delay, Hypotonia, and Short Stature;Pediatric Reports;2022-12-05

3. Autistic Traits and Obsessive-Compulsive Disorder in Patients with Migraine With or Without Aura;Psychiatry and Behavioral Sciences;2022

4. The spectrum of epilepsy in children with 15q13.3 microdeletion syndrome;Seizure;2021-11