نتایج جستجو برای: peters anomaly

تعداد نتایج: 42218  

2018
Sangwan PARK Kiwoong KIM Youngbeum KIM Kangmoon SEO

A seven-month-old female domestic shorthaired cat was presented for buphthalmos in the right eye and corneal cloudiness in the left eye. Full ophthalmic examinations were performed for both eyes and enucleation was done for the right nonvisual eye. Congenital glaucoma caused by anterior segment dysgenesis was confirmed for the right eye. In the left eye, slit-lamp examination revealed focal cor...

Journal: :The Journal of clinical investigation 2009
Keiichiro Iwao Masaru Inatani Yoshihiro Matsumoto Minako Ogata-Iwao Yuji Takihara Fumitoshi Irie Yu Yamaguchi Satoshi Okinami Hidenobu Tanihara

During human embryogenesis, neural crest cells migrate to the anterior chamber of the eye and then differentiate into the inner layers of the cornea, the iridocorneal angle, and the anterior portion of the iris. When proper development does not occur, this causes iridocorneal angle dysgenesis and intraocular pressure (IOP) elevation, which ultimately results in developmental glaucoma. Here, we ...

2017
Reiichiro SATO Ken ONDA Masaru MURAKAMI Daiya ITO Hiroo MADARAME

A Holstein calf was born with a large protruding right eye and a central corneal opacity. Enucleation was the first choice of treatment. The calf had a good prognosis and was raised for milking purposes. Macroscopically, the enucleated eye was characterized by the protruded cornea, adherence of the iris to the central posterior cornea and aphakia. Microscopically, central corneal thickening and...

Journal: :Psychiatric Bulletin 2008

Journal: :Diabetes 2002
Tetsuyuki Yasuda Yoshitaka Kajimoto Yoshio Fujitani Hirotaka Watada Shuji Yamamoto Takao Watarai Yutaka Umayahara Munehide Matsuhisa Shin-ichi Gorogawa Yasuaki Kuwayama Yasuo Tano Yoshimitsu Yamasaki Masatsugu Hori

A paired homeodomain transcription factor, PAX6, is a well-known regulator of eye development, and its heterozygous mutations in humans cause congenital eye anomalies such as aniridia. Because it was recently shown that PAX6 also plays an indispensable role in islet cell development, a PAX6 gene mutation in humans may lead to a defect of the endocrine pancreas. Whereas heterozygous mutations in...

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