CONGENITAL entropion is a rare malformation of the eyelid and for that reason this case is worth publishing. Among the 160,000 patients of the University Eye Clinic Debrecen in the last 25 years many cases of epiblepharon have been observed, but among them this is the only one in which we had to deal with real entropion.

While conducting medical aid in Mozambique, a 41 year old African male presented to our eye clinic complaining of visual impairment. The male was found to have Peters' anomaly type 2, a rare congenital ocular malformation leading to sensory amblyopia and glaucoma.

Congenital cystic Adenomatoid malformation is a rare developmental abnormality of the lung occuring in 1-4/100000 live births.In most cases the outcome with CCAM in fetus is very good,while in some cases the outcome is very bad and can be life threatning for the fetus.we report here a case of 40 day old female infant who presented with worsening respiratory distress since birth and x ray and CT...

An unusual retinal arterial malformation is presented in this case report. A 50-years-old female with no significant past medical history, presented with an unusual retinal arterial malformation without any vision loss in the right eye. Inferior temporal retinal artery had a corkscrew like looping and extension to vitreous cavity at its emerging site from optic disc. Fundus fluorescein angiogra...

Congenital ocular malformation may lead to failure of the development of ocular regions and visual function in the pediatric population. Orbital bones are established within the first 2 months of embryogenesis. Any abnormalities may lead to failure in development of the ocular region. In this case report, we present a newborn with congenital canthus malposition, a distorted tarsus, and mild eno...

background the most common space occupying lesions of the fetal thorax are congenital diaphragmatic hernia (cdh), congenital cystic adenomatoid malformation (ccam), and bronchopulmonary sequestration (bps). although applications of prenatal mri have been vastly improved in the recent years, its use in the assessment of space occupying lesions of the fetal chest differs among centers. objectives...

BACKGROUND AND OBJECTIVES Walker-Warburg Syndrome is a rare, autosomal recessive congenital muscular dystrophy manifested by central nervous system, eye malformations and possible multisystem involvement. The diagnosis is established by the presence of four criteria: congenital muscular dystrophy, type II lissencephaly, cerebellar malformation, and retinal malformation. Most of the syndromic ch...

malformations which occur during the development of the avian body organs can lead to structural and functional abnormalities. most defects are recognized at hatching, but some go undetected until somewhat later. the cause of the majority of animal congenital malformations is unknown. a significant proportion of congenital malformations of unknown cause are likely to have an important genetic c...

holt-oram syndrome (hos) is a developmental disorder inherited in an autosomal-dominant pattern. affected organs are the heart and forelimbs with upper extremity skeletal defects and congenital heart malformation. in this study we present three cases of hos in the same family. in one of these three individuals we detected a transition of c to t (ctg-gtt, v205v) in exon 7 of the tbx5 gene. this ...

a 5-day-old female holstein calf was necropsied because of lethargy, recumbency and anorexia. at necropsy, multiple gross defects were evident in several organs, including unclosed sutures of skull bones, asymmetrical orbits, doming of the skull bones, hydrocephalus, hydranencephaly, cleft palate, brachygnathia, ventricular septal defect, mitral valve dysplasia and rudimentary lungs. on microsc...