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.
Primary Language | English |
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Subjects | Health Care Administration |
Journal Section | Case Reports |
Authors | |
Publication Date | September 30, 2018 |
Acceptance Date | July 10, 2018 |
Published in Issue | Year 2018Volume: 40 Issue: 3 |