[Familial hyperinsulinism].

Abstract:

:The authors present the case history of a 2 year old child suffering from nesidioblastosis. Severe non-ketotic symptomatic hypoglycaemia developed within the first hour of birth. Diagnosis of nesidioblastosis was confirmed by high insulin concentration accompanying hypoglycaemia, the increase in blood glucose level after glucagon administration and the stabilization of blood glucose level by continuous high rate glucose infusion. Normal blood glucose concentration was achieved by combined medical treatment (diazoxide, chlorothiazide and prednisolone) and the administration of starch. The authors present by familial form of the disease with autosomal recessive inheritance pattern and stress the significance of the intrauterine diagnosis. They summarize the main diagnostic and therapeutical management of the disease with special emphasize of the early intervention in order to prevent severe brain damage.

journal_name

Orv Hetil

journal_title

Orvosi hetilap

authors

Lásztity N,Balogh L

subject

Has Abstract

pub_date

1995-07-23 00:00:00

pages

1611-3

issue

30

eissn

0030-6002

issn

1788-6120

journal_volume

136

pub_type

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  • [Health behavior change: motivational interviewing].

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  • [Presence of antibodies to human herpesvirus type 6 and 7 in Hungarian children].

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  • [Most common skin disorders caused by excessive exposure to sunlight].

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  • [Experience with saphenous-peritoneal shunts in the treatment of intractable ascites].

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  • [Surgical ventricular reconstruction for ischemic left ventricular aneurysm. Early and medium-term outcomes for two surgical techniques].

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  • [Heterotaxy syndrome, analysis of 13 cases and review of the literature].

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  • [Tissue Doppler imaging in the assessment of right ventricular function in congenital heart disease. Correlation with echo-MRI].

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  • [Prenatal follow-up of fetal tachyarrhythmia].

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