婴儿无症状高钠血症与中线缺陷。

EJIFCC Pub Date : 2021-12-07 eCollection Date: 2021-12-01
Sangeetha Geminiganesan, Padmasani Venkat Ramanan, Dhivyalakshmi J, Bhogavalli Lakshmi Harshita, Deepalakshmi Sriram
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引用次数: 0

摘要

无前脑畸形是由于胚胎发生早期吻侧神经管(基底前脑)结构不完全劈裂而引起的发育异常。这种缺陷导致左右脑半球不完全分离。儿童表现出广泛的临床表现,其程度取决于半球不分离的程度。我们描述了一个婴儿与中线裂参考术前评估,其中无症状电解质异常和前脑全畸形被确定。经进一步评估,婴儿被诊断为孤立的中枢性尿崩症,她对口服去氨加压素治疗反应良好。唇腭裂是最常见的先天性畸形之一,中线裂可能与显著的垂体异常有关。意识到与唇裂和相关异常的综合征关联对于这些儿童的早期诊断和干预是重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Asymptomatic Hypernatremia in an Infant with Midline Defects.

Asymptomatic Hypernatremia in an Infant with Midline Defects.

Asymptomatic Hypernatremia in an Infant with Midline Defects.

Holoprosencephaly is a developmental abnormality caused due to incomplete cleavage of the rostral neural tube (basal forebrain) structures during early embryogenesis. This defect causes incomplete separation of the right and left cerebral hemispheres. Children manifest a wide spectrum of clinical manifestations, the extent of which depends upon the degree of hemispheric nonseparation. We describe an infant with midline cleft referred for preoperative evaluation in whom, asymptomatic electrolyte abnormalities and holoprosencephaly were identified. On further evaluation, the infant was diagnosed to have isolated central diabetes insipidus and she responded well to oral desmopressin therapy. Cleft lip and palate is one of the commonest congenital malformations and midline clefts are likely to be associated with significant pituitary abnormalities. Awareness about the syndromic associations with clefts and the associated anomalies are important for early diagnosis and intervention in these children.

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