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先天性胰岛缺失。

Congenital absence of islets of Langerhans.

作者信息

Dodge J A, Laurence K M

出版信息

Arch Dis Child. 1977 May;52(5):411-3. doi: 10.1136/adc.52.5.411.

Abstract

A small-for-dates male infant who developed acute metabolic acidosis shortly after birth had diabetes and died aged 40 hours. At necropsy there was an absence of any recognizable islets of Langerhans though lymphorecticular aggregates were found. This was the fourth child of healthy unrelated parents whose first child, also a male, died at 48 hours under similar circumstances. It is suggested that both boys had the same underlying pathology and this might be a previously undescribed recessive or x-linked inherited condition.

摘要

一名出生体重低于孕周的男婴出生后不久出现急性代谢性酸中毒,患有糖尿病,于40小时时死亡。尸检时未发现任何可识别的朗格汉斯胰岛,但发现有淋巴网状细胞聚集。这是一对健康非近亲父母的第四个孩子,他们的第一个孩子也是男孩,在类似情况下于48小时时死亡。据推测,两个男孩都有相同的潜在病理,这可能是一种以前未描述过的隐性或X连锁遗传性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4939/1544555/0051a909adff/archdisch00817-0077-a.jpg

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