[全前脑畸形伴神经源性高钠血症]
[Holoprosencephaly with neurogenic hypernatremia].
作者信息
Cuisset J M, Cuvellier J C, Vallée L, Ryckewäert P, Soto-Ares G, Nuyts J P
机构信息
Service des maladies infectieuses et de neurologie infantiles, CHRU de Lille, hôpital Roger-Salengro, Lille.
出版信息
Arch Pediatr. 1999 Jan;6(1):43-5. doi: 10.1016/S0929-693X(99)80072-4.
BACKGROUND
Semi-lobar holoprosencephalies can be seldom complicated by neurogenic hypernatremia, which must be distinguished from other causes of hypernatremia.
CASE REPORT
In two admitted children with semi-lobar holoprosencephaly, 7 months and 4 years old, biological data revealed chronic hypernatremia and hyperosmolarity without clinical signs of dehydration, which were finally attributed to a neurogenic hypernatremia.
CONCLUSION
Neurogenic hypernatremia must be clearly differentiated from other causes of hypernatremia since it never causes specific complications.
背景
半侧脑叶型全前脑畸形很少并发神经源性高钠血症，必须将其与高钠血症的其他病因区分开来。
病例报告
两名分别为7个月和4岁的半侧脑叶型全前脑畸形患儿入院，生物学数据显示存在慢性高钠血症和高渗状态，但无脱水的临床体征，最终归因于神经源性高钠血症。
结论
必须将神经源性高钠血症与高钠血症的其他病因明确区分，因为它从不引起特定并发症。
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