非近亲结婚中的 COFS 综合征

Maryam Mefarreh, Yousef Mohammad, Tarek Nabil, Mahmoud Ahmed Shokeir
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引用次数: 0

摘要

脑-眼-面-骨骼(COFS)综合征是一种罕见的遗传性疾病,每 100 万个出生的胎儿中就有一个会患病。其遗传方式为常染色体隐性遗传(AR)。COFS 综合征影响身体的各个系统,患儿的寿命为 3-5 岁。呼吸道感染和喂养困难是这些患者发病率和死亡率增加的主要原因。需要强调的是,这种综合征的表现可能与传染性胎儿病(巨细胞病毒、风疹和弓形虫病)、13 三体综合征和 18 三体综合征相似。
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COFS Syndrome in a Non-Consanguineous Marriage
Cerebro-Oculo-Facio-Skeletal (COFS) syndrome is a rare genetic disorder affecting 1 in 1,000,000 born fetuses. Its mode of inheritance is autosomal recessive (AR). COFS syndrome affects various systems within the body, and the life span of children born with the disease is between 3-5 years. Respiratory infections and feeding difficulties are the main causes of the increased morbidity and mortality in these patients. It is important to highlight this syndrome as it may present similarly to infectious fetopathies (cytomegalovirus, rubella, and toxoplasmosis), trisomy 13 and 18
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