Synonymer & Anagram | Engelska ordet ECTOPIA

Exempel på hur man kan använda ECTOPIA i en mening

• Cerebellar tonsillar ectopia, aka Chiari malformation, a herniation of the brain through the foramen magnum, which may be congenital or caused by trauma.
• Lower levels of mRNA expression were associated with a higher risk for ectopia lentis, the displacement of the crystalline lens of the eye, and pectus deformity, an abnormality of the chest muscle, indicating that variation in expression could be due to levels of expressivity and not genotype.
• Hyperlysinemia is associated with ectopia lentis (a displacement or malposition of the eye's crystalline lens) in humans.
• There was a case of a 28-month-old with renal ectopia who showed an absence of the gluteal muscle with no spina bifida occulta.
• Abnormal development of these zonules can lead to primary ectopia lentis, usually a bilateral condition.
• If the sternal defect is large enough, the neonate may have ectopia cordis, in which the heart is located outside of the thorax.
• The diagnosis of ectopia cordis is found with a routine ultrasound as early as the first trimester or the beginning of the second trimester.
• It is characterized by aniridia, ectopia lentis, abnormal upper incisors and intellectual disability.
• The eye manifestations typically include unusually small, round lenses of the eyes (microspherophakia), which may be prone to dislocating (ectopia lentis), as well as other ocular defects.
• but are more than twice as effective at diagnosing cerebellar tonsillar ectopia, also known as Chiari malformation.
• Other conditions associated with mutations in this gene include acromicric dysplasia, Marfan syndrome and its variant Marfanoid–progeroid–lipodystrophy syndrome, autosomal dominant Weill-Marchesani syndrome, isolated ectopia lentis, MASS phenotype, and Shprintzen-Goldberg syndrome.
• As a congenital malformation or ectopia, it is distinctly different from the trauma or iatrogenic development of an encephalocele.
• Blepharoptosis-myopia-ectopia lentis syndrome is an extremely rare genetic disorder which is characterized by congenital bilateral blepharoptosis, presence of ectopia lentis, and severe near-sightedness (myopia).
• Crowhurst was born with autosomal dominant congenital nystagmus and cataracts with Anterior Segment Developmental Anomalies (ASDA) with ectopia pupillae and Zonular weakness.
• Although no other ocular abnormalities are present in isolated ectopia lentis, the EL itself can lead to other ocular complications directly or indirectly related to it, such as myopia, astigmatism, hyperopia, cataract, glaucoma, and retinal detachment, which may lead to visual impairment (difficulties with vision) or even total blindness.
• Radio-renal syndrome is a rare, presumably autosomal dominant genetic disorder characterized by underdevelopment of the digits as a result of the maldevelopment of either the radius, ulnae, or both, alongside renal ectopia, renal agenesis, mild malformations of the external ear, short stature.

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