Literature DB >> 26917672

Congenital Mirror Movements in Gorlin Syndrome: A Case Report With DTI and Functional MRI Features.

Erdal Sag1, Rahsan Gocmen2, F Gokcem Yildiz3, Zeynelabidin Ozturk4, Cagri Temucin5, Ozlem Teksam4, Eda Utine6.   

Abstract

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.
Copyright © 2016 by the American Academy of Pediatrics.

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Year:  2016        PMID: 26917672     DOI: 10.1542/peds.2015-1771

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  1 in total

1.  Unusual Neurological Presentation of Nevoid Basal Cell Carcinoma Syndrome (Gorlin-Goltz Syndrome).

Authors:  Manuela Pennisi; Giuseppe Lanza; Mariagiovanna Cantone; Carmelo Schepis; Raffaele Ferri; Rita Barone; Rita Bella
Journal:  J Clin Neurol       Date:  2017-09-04       Impact factor: 3.077

  1 in total

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