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A Rare Syndrome and a Rare Association: Dandy-Walker Malformation and Cockayne Syndrome in a Child 

Isikay, Sedat; Bilgin, Burak; Karaer, Kadri; Sirikci, Akif (GEORG THIEME VERLAG KG, 2019-04)
Cockayne syndrome is a rare autosomal recessive, neurodegenerative disorder characterized by a broad spectrum of clinical symptoms. Herein, we will describe a patient diagnosed with Cockayne syndrome by genetic testing who ...



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AuthorBilgin, Burak (1)
Isikay, Sedat (1)
Karaer, Kadri (1)Sirikci, Akif (1)SubjectCockayne syndrome; Dandy-Walker malformation; child (1)... View MoreDate Issued
2019 (1)
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