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Your search keyword '"Zengın, Neslihan"' showing total 4 results
Start Over Author "Zengın, Neslihan" Publication Type Academic Journals
4 results on '"Zengın, Neslihan"'

1. Mortality risk factors among critically ill children with MIS-C in PICUs: a multicenter study

Author

Sık, Guntulu, Inamlık, Aysegul, Akçay, Nihal, Kesici, Selman, Aygun, Fatih, Kendırlı, Tanıl, Atay, Gurkan, Sandal, Ozlem, Varol, Fatih, Ozkaya, Pınar Yazıcı, Duyu, Muhterem, Bırbılen, Ahmet Ziya, Ozcan, Serhan, Arslan, Gazi, Kangın, Murat, Bayraktar, Suleyman, Altug, Umit, Anıl, Ayşe Berna, Havan, Merve, Yetımakman, Ayse Filiz, Dalkıran, Tahir, Zengın, Neslihan, Oto, Arzu, Kıhtır, Hasan Serdar, Gırgın, Feyza İnceköy, Telhan, Leyla, Yıldızdas, Dincer, Yener, Nazik, Yukselmıs, Ufuk, Alakaya, Mehmet, Kılınc, Mehmet Arda, Celegen, Mehmet, Dursun, Adem, Battal, Fatih, Sarı, Ferhat, Ozkale, Murat, Topal, Sevgi, Kocaoglu, Celebi, Yazar, Abdullah, Alacakır, Nuri, Odek, Caglar, Yaman, Ayhan, and Cıtak, Agop

Published
2023
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4. Akromatopsili İki Olgunun İrdelenmesi.

Author

Zengın, Mehmet Özgür, Doğan, Beysim, Zengın, Neslihan, and Men, Gamze

Subjects
*COLOR blindness, *VISUAL acuity, *SCOTOMA, *COLOR vision, *VISION disorders, *COUNSELING
Abstract

Achromatopsia is a rare, inherited condition characterized by reduced visual acuity, photophobia, small central scotoma and total or partial loss of color vision. Electroretinograghy (ERG) recordings and psychophysical tests typically show a complete absence of cone function. In this study we described two cases, a 32-years-old woman and her seven-years-old daughter, who presented with visual impairment and photophobia. Early diagnosis of diseases that have characteristic clinical findings like Achromatopsia is important for genetic counselling. [ABSTRACT FROM AUTHOR]

Published
2012

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