Cranial MRI findings in a case with Seckel syndrome
Abstract
Özet
Seckel sendromu (SS) nadir, heterojen bir primordiyal cücelik türüdür. Zeka geriliği ve nörolojik belirtilerin varlığı bu sendromun kendine has özelliklerinden biridir. Biz burada Seckel sendromlu bir çocuk hastada kraniyal MR bulgularını sunuyoruz.
Abstract
Seckel’s syndrome (SS) is a rare, heterogeneous form of primordial dwarfism. The presence of mental retardation and neurologic signs is one of the peculiar features of this syndrome. We herein present the cranial MR findings in a child patient with Seckel's syndrome.
Keywords
References
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Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Case Report
Authors
Mehmet Atalar
*
Türkiye
Publication Date
September 30, 2018
Submission Date
April 22, 2018
Acceptance Date
July 10, 2018
Published in Issue
Year 2018 Volume: 40 Number: 3