Congenital Mirror Movements in Gorlin Syndrome: A Case Report With DTI and Functional MRI Features
| Autor: | Ozturk Z, Teksam O, Utine E, Yildiz Fg, Temucin C, Rahsan Gocmen, Erdal Sag |
|---|---|
| Přispěvatelé: | Çocuk Sağlığı ve Hastalıkları |
| Rok vydání: | 2015 |
| Předmět: |
0301 basic medicine
Male Pathology medicine.medical_specialty Movement disorders Adolescent Basal Cell Nevus Syndrome Nevoid basal-cell carcinoma syndrome Mirror movements Pediatrics 03 medical and health sciences 0302 clinical medicine medicine Humans Basal cell carcinoma Movement Disorders medicine.diagnostic_test business.industry Genetic disorder Magnetic resonance imaging Anatomy medicine.disease Magnetic Resonance Imaging stomatognathic diseases 030104 developmental biology Diffusion Tensor Imaging Pediatrics Perinatology and Child Health medicine.symptom business 030217 neurology & neurosurgery Diffusion MRI |
| Zdroj: | Pediatrics. 137(3) |
| ISSN: | 1098-4275 |
| Popis: | Congenital mirror movements are rare conditions that define the inability to perform unimanual movements. Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with multiple nevi predisposing to basal cell carcinoma, odontogenic keratocysts, and skeletal malformations. Herein we report on an adolescent patient with Gorlin syndrome and coexisting congenital mirror movements. To our knowledge, this is the first patient in the literature who has both of these very rare conditions. |
| Databáze: | OpenAIRE |
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