1例诊断为染色体18p11.1微缺失综合征的新生儿患者表现为18三体样表型。

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2023-01-01 DOI:10.1155/2023/2275582
Deepa Banker, Bhavdeep Mungala, Zankhana Parekh, Shachi Ganatra, Vimal Maheshwari, Yashica Raj, Utsav Patel, Digant Patel, Kishan Chamar, Vasu Solanki
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引用次数: 0

摘要

18号染色体短臂微缺失是最常见的染色体缺失综合征之一。据估计,其发病率为每5万名活产婴儿中有1例,女性患病率高于男性。到目前为止,已发现约150例病例。报告的异常包括生长缺陷、张力低下、小头畸形、面部畸形,如上睑下垂、表皮褶皱、远端肥大和小颌,以及相对较小的手和脚。我们的病人是一个足月低出生体重(2150克)的女婴,表现为上唇和上颚(软硬腭)裂,双侧先天性马蹄足内翻伴摇底足,小头畸形,房间隔缺损。患者最初采用灌胃保守喂养,随后改为宫殿式母乳喂养。由于各种畸形和潜在的并发症,采用了多学科的方法。据我们所知,这是新生儿期确诊的首例病例。
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A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype.

Microdeletion of the short arm of chromosome 18 is one of the most common chromosome deletion syndromes. Its estimated frequency is 1 in 50,000 live-born infants, with female prevalence over males. Around 150 cases have been described till now. The reported abnormalities include growth deficiency, hypotonia, microcephaly, dysmorphic facial features such as ptosis, epicanthal folds, hypertelorism and micrognathia, and relatively small hands and feet. Our patient was a full-term low birth weight (2150 gm) female newborn, showing cleft upper lip and palate (hard and soft palate), bilateral congenital Talipes Equinovarus with rocker bottom foot, microcephaly, atrial septal defect. She was initially conservatively managed with gavage feeding, then shifted into paladai feeding of expressed breast milk. A multidisciplinary approach was adopted due to various malformations and for the potential occurring complications. To our knowledge, this is the first case diagnosed during the neonatal period.

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自引率
11.10%
发文量
48
审稿时长
13 weeks
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