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[Congenital hyperinsulinism as a part of Kabuki syndrome].
- Source :
-
Problemy endokrinologii [Probl Endokrinol (Mosk)] 2022 Jul 20; Vol. 68 (5), pp. 91-96. Date of Electronic Publication: 2022 Jul 20. - Publication Year :
- 2022
-
Abstract
- Kabuki syndrome is a rare hereditary disease characterized by distinctive facial features, skeletal abnormalities, mental retardation, developmental delay, and anomalies in multiple organ systems development.Congenital hyperinsulinism is a rare manifestation of his Kabuki syndrome. However, early diagnosis is crucial to prevent neurological complications of hypoglycemia.There are 2 types of Kabuki Syndrome depending on severity of symptoms. Kabuki syndrome Type 1 is associated with heterozygous mutations in gene KMT2D. Kabuki syndrome Type 2 is inherited in an X-linked manner. It's associated with heterozygous mutations in gene KDM6A and characterized by more severe course of the disease.This paper presents 2 cases of children with congenital hyperinsulinism as the feature of Kabuki syndrome Type 1 and Type 2.
- Subjects :
- Child
Humans
Vestibular Diseases complications
Vestibular Diseases diagnosis
Vestibular Diseases genetics
Hematologic Diseases complications
Hematologic Diseases diagnosis
Hematologic Diseases genetics
Abnormalities, Multiple genetics
Abnormalities, Multiple diagnosis
Congenital Hyperinsulinism complications
Congenital Hyperinsulinism diagnosis
Congenital Hyperinsulinism genetics
Subjects
Details
- Language :
- Russian
- ISSN :
- 2308-1430
- Volume :
- 68
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Problemy endokrinologii
- Publication Type :
- Academic Journal
- Accession number :
- 36337023
- Full Text :
- https://doi.org/10.14341/probl13145