These cases were diagnosed as Seckel syndrome and presented here because the syndrome is very rare and the cases had all the major criteria so far re¬ported for this syndrome.
📌 3 Key Takeaways
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Objective & Hypothesis:Two cases with severe mental retardation and microcephaly were admitted to the Pediatrics Department of Çukurova University Hospital and examined in the Genetics Unit.
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Key Findings & Data:Two cases with severe mental retardation and microcephaly were admitted to the Pediatrics Department of Çukurova University Hospital and examined in the Genetics Unit.
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Conclusion & Impact:These cases were diagnosed as Seckel syndrome and presented here because the syndrome is very rare and the cases had all the major criteria so far re¬ported for this syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Two cases with severe mental retardation and microcephaly were admitted to the Pediatrics Department of Çukurova University Hospital and examined in the Genetics Unit. These cases were diagnosed as Seckel syndrome and presented here because the syndrome is very rare and the cases had all the major criteria so far re¬ported for this syndrome.
Özet
Çukurova Üniversitesi Hastanesi Pediatri Polikliniğine getirilen ileri derecede mental retarde ve mikrosefalik iki olgu genetik yönden incelendi, Seckel sendromu tanısı konan olgular, bu sendromun tüm major kriterlerini bulundurması ve sendromun nadir görülmesi nedeniyle sunuldu.
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Cite This Article
TEMOÇİN, A. K., EVLİYAOĞLU, N., ALTINTAŞ, D. V., YEĞİN, A., ALTINBAŞAK, Ş. (2022). Seckel syndrome. Erciyes Tıp Dergisi, Cilt: 17 - Sayı: 2, 166–169. https://ajindex.com/articles/503119