Congenital hyperinsulinism: clinical cases
Background. Congenital hyperinsulinism (CHI) is a hereditary disorder presenting with the hypersecretion of insulin by pancreatic beta cells and further development of hypoglycaemia. CHI is an orphan disease. According to the European sources, its incidence averages to 1:30,000– 1:50,000 newborns.Cl...
Saved in:
Main Authors: | I. Yu. Chernyak, E. I. Kleshchenko, E. M. Shadrina, A. S. Alekseenko, I. M. Golovenko |
---|---|
Format: | Article |
Language: | Russian |
Published: |
Ministry of Healthcare of the Russian Federation. “Kuban State Medical University”
2022-05-01
|
Series: | Кубанский научный медицинский вестник |
Subjects: | |
Online Access: | https://ksma.elpub.ru/jour/article/view/2669 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A clinical case of congenital hyperinsulinism in an early child
by: S. B. Berezhansky, et al.
Published: (2020-09-01) -
NEUROLOGICAL PAROXYSMAL DISORDERS IN CHILDREN WITH HYPOGLYCEMIA IN CONGENITAL HYPERINSULINISM: POLYMORPHISM OF CLINICAL IMPLICATIONS
by: I. O. Shchederkina, et al.
Published: (2016-05-01) -
Congenital hyperinsulinism associated with Hirschsprung’s disease—a report of an extremely rare case
by: Takeshi Shono, et al.
Published: (2020-01-01) -
Identification of an ABCC8 variant in a kindred with transient diazoxide responsive hyperinsulinism
by: Ryan L Smith, et al.
Published: (2025-07-01) -
Clinical and morphological differential diagnosis of congenital hyperinsulinism before the stage of immunohistochemical study of paraffin-embedded specimens of pancreas in children
by: A. A. Perminova, et al.
Published: (2021-02-01)