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De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: A case report

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Tos, Tülay
Alp, Muhammed Yunus
Karacan, Can Demir
Andıran, Nesibe
Çolakoglu, E. Y.

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Medecine Et Hygiene

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De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: a case report: In this report we describe a 10 year-old female patient with interstitial deletion of 9q32-q34.1 associated with mental retardation, developmental delay, short stature, mild facial dysmorphism, epilepsy, abnormal EEG and brain MRI findings consistent with focal cortical dysplasia. Interstitial deletion of 9q associated with q32-q34 is found extremely rare. Common features of seven previously reported cases are mental retardation, developmental delay, short stature, a distinct cranial and facial phenotype (brachycephaly, low midface, low and prominent forehead, and low set malformed ears). Combination of epilepsy, abnormal EEG and brain MRI findings are not reported before.

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Cortical dysplasia, Mental retardation, Developmental delay, Interstitial deletion 9q32-q34.1, Epilepsy, Biotechnology & applied microbiology, Genetics & heredity, Research & experimental medicine, Medical ethics

Alıntı

Tos, T. vd. (2014). "De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: A case report". Genetic Counseling, 25(2), 197-201.

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