نتایج جستجو برای: microphthalmos

تعداد نتایج: 826  

Journal: :Animal genetics 2007
S M Schmutz T G Berryere

Tremendous progress has been made in identifying genes involved in pigmentation in dogs in the past few years. Comparative genomics has both aided and benefited from these findings. Seven genes that cause specific coat colours and/or patterns in dogs have been identified: melanocortin 1 receptor, tyrosinase related protein 1, agouti signal peptide, melanophilin, SILV (formerly PMEL17), micropht...

2016
Jing Li Shusheng Wang Chastain Anderson Fangkun Zhao Yu Qin Di Wu Xinwei Wu Jia Liu Xuefei He Jiangyue Zhao Jinsong Zhang

Microphthalmia is characterized by abnormally small eyes and usually retinal dysplasia, accounting for up to 11% of the blindness in children. Right now there is no effective treatment for the disease, and the underlying mechanisms, especially how retinal dysplasia develops from microphthalmia and whether it depends on the signals from lens ectoderm are still unclear. Mutations in genes of the ...

Journal: :Archives of disease in childhood 1976
J E Brice

An infant with left microphthalmia, enophthalmia, and cataract with scattered zosterform skin lesions from maternal varicella at 20 weeks' gestation is described. The mother's abnormal obstetric history is discussed and published reports on congenital and neonatal varicella reviewed.

2015
Ahmad A Albar Sawsan R Nowilaty Nicola G Ghazi

PURPOSE Novel spectral-domain optical coherence tomography (SD-OCT) findings in posterior microphthalmos (PM) include cystoid changes in the papillomacular fold (PMF). These changes may be misdiagnosed as cystoid macular edema (CME) and may trigger unnecessary treatment including intravitreal injections. We report a case that underscores this scenario aiming to increase awareness of this entity...

Journal: :Korean journal of ophthalmology : KJO 2005
Un Chul Park Ho Kyung Choung Seong Joon Kim Young Suk Yu

PURPOSE Protein C deficiency is an autosomal recessive disorder, which predisposes the patient to potentially blinding and widespread lethal thromboembolic complications, especially in the homozygous type. We here report the first Korean case of ophthalmic involvement and its surgical treatment in homozygous protein C deficiency. METHODS A 3.4kg, full term girl was born by normal delivery but...

Journal: :Archives of ophthalmology 2001
I Anteby E Cohen E Anteby D BenEzra

OBJECTIVE To report the ocular abnormalities found in children born after in vitro fertilization. METHODS Forty-seven children (25 girls and 22 boys) born after an in vitro fertilization pregnancy (mean +/- SD birth weight, 2335 +/- 817 g; range, 924-4300 g) and referred for ophthalmic evaluation were included in the study. All underwent a thorough ocular examination. Obstetric history was ga...

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