التفاصيل البيبلوغرافية
| العنوان: |
Imagawa-Matsumoto Syndrome: The First Case From Turkey. |
| المؤلفون: |
YÜCEL, Zeliha, YÜKSEL, Emine Berrin, KOÇ, Altuğ |
| المصدر: |
Archives of Neuropsychiatry / Nöropsikiyatri Arşivi; Sep2024, Vol. 61 Issue 3, p289-292, 4p |
| مصطلحات موضوعية: |
BEHAVIOR disorders, CEREBRAL cortex abnormalities, NEURAL development, CHROMOSOME abnormalities, MUSCULOSKELETAL system abnormalities, MAGNETIC resonance imaging, INTELLECTUAL disabilities, AGENESIS of corpus callosum, MICROARRAY technology, CRANIOFACIAL dysostosis, GENETIC mutation |
| مصطلحات جغرافية: |
TURKEY |
| مستخلص: |
Imagawa-Matsumoto syndrome (IMMAS; MIM #618786) is an autosomal dominant syndrome characterized by overgrowth, dysmorphic features, musculoskeletal abnormalities, developmental delay, and intellectual disability. The first case was reported in 2017 and has subsequently been diagnosed in only another 12 patients. We also present the first IMMAS patient from Turkey. A 19-year-old female was admitted to the neurology outpatient clinic due to a behavioral disorder and intellectual disability. Her physical examination revealed macrocephaly and dysmorphic features like a round face, broad forehead, hypertelorism, and variable skeletal anomalies such as flat feet, clinodactyly, and macrocephaly. Cranial magnetic resonance imaging (MRI) showed agenesis of the corpus callosum and polymicrogyria. Chromosomal analysis results were consistent with a normal constitutional female karyotype and microarray analysis showed a de novo 1.5-MB size deletion on the long arm of chromosome 17; band q11.2 encompassing the Polycomb Repressive Complex 2 Subunit (SUZ12 gene, MIM *606245). This report will contribute to the limited information in the literature. [ABSTRACT FROM AUTHOR] |
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