نتایج جستجو برای: microphthalmia

تعداد نتایج: 1639  

Journal: :American Journal of Medical Genetics Part A 2010

Journal: :journal of nursing and midwifery sciences 0
mehrbanu amirshahi faculty of nursing & midwifery, zabol university of medical sciences, zabol, iran akram sanagoo nursing research center, golestan university of medical sciences, golestan, iran ashraf salehi faculty of medical sciences khomain, arak university of medical sciences arak, iran azam kerami faculty of medical sciences khomain, arak university of medical sciences arak, iran abdolghani abdollahimohammad faculty of nursing & midwifery, zabol university of medical sciences, zabol, iran fatemeh mirshekari faculty of nursing & midwifery, zabol university of medical sciences, zabol, iran

holoprosencephaly (hpe) is a rare congenital brain malformation associated with multiple midline facial defects. this anomaly is resulted from the failure of diverticulation and cleavage of primitive prosencephalon during weeks 4-8 of gestation. hpe is the most common forebrain developmental anomaly in human with the incidence rate of 0.49-1.2 cases per 10,000-20,000 term births. in this study,...

Journal: :Journal of Nepal Medical Association 2019

2010
Annaïck Desmaison Adeline Vigouroux Claudine Rieubland Christine Peres Patrick Calvas Nicolas Chassaing

PURPOSE Microphthalmia and anophthalmia are at the severe end of the spectrum of abnormalities in ocular development. A few genes (orthodenticle homeobox 2 [OTX2], retina and anterior neural fold homeobox [RAX], SRY-box 2 [SOX2], CEH10 homeodomain-containing homolog [CHX10], and growth differentiation factor 6 [GDF6]) have been implicated mainly in isolated micro/anophthalmia but causative muta...

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