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循环病,一种罕见而致命的先天性异常:两例病例报告,2025年
Berhe Tesfai1, Hailemichael Gebremariam2, Abraham Amanuel Gebrezgabhier3
1Department of Obstetrics and Gynaecology, Orotta National Referral Maternity Hospital, Maekel Region, Asmara, Eritrea.
International medical case reports journal
|February 19, 2026
概括
环眼症是一种罕见的先天性异常,导致只有一只眼睛,是致命的. 早期产前超声检测对于患者咨询至关重要,特别是在资源有限的环境中.
科学领域:
- 医学遗传学 医学遗传学
- 发育生物学 发展生物学
- 新生儿科学 新生儿科学
背景情况:
- 环眼症是一种极其罕见的,致命的先天性异常,其特点是眼球轨道分裂失败,导致单个或紧密位置的眼球场.
- 循环的确切原因尚不清楚.
- 患有循环病的婴儿的预后很差,大多数婴儿在出生后不久或在婴儿时期死亡.
研究的目的:
- 为了呈现两例产后诊断的循环病例.
- 强调产前超声波对于检测先天性异常的重要性.
- 突出需要在资源有限的环境中改进诊断能力.
主要方法:
- 在两个新生儿中,产后诊断出循环.
- 对外部先天性异常进行临床检查.
- 对诊断和预后影响的审查.
主要成果:
- 在分娩后发现了两例循环眼症,其特点是单一的中心眼睛和鼻.
- 一个病例也出现了囊性湿原.
- 这两个婴儿在出生后不久就去世了.
结论:
- 详细的产前超声波扫描对于早期检测循环病和其他先天异常是必不可少的.
- 早期诊断有助于更好地为患者提供咨询.
- 常规的产前超声波在资源较低的国家特别重要,可以及时识别胎儿的异常.
相关概念视频
Nondisjunction
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Genomic Imprinting and Inheritance
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Lethal Alleles
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Centrosome Duplication
The primary microtubule organizing center (MTOC) in animal cells is the centrosome. A centrosome has two cylindrical centrioles at its core. Each centriole consists of nine sets of three microtubules held together by proteins. The centrioles are positioned at right angles to each other and surrounded by a shapeless protein cloud called the pericentriolar matrix, or pericentriolar material (PCM).
To ensure that each daughter cell receives a centrosome after cell division, centrosome duplication...
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Nondisjunction
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...

