Kabuki syndrome associated with type 1 diabetes mellitus: report of three cases

Kabuki syndrome is a rare genetic disorder characterized by distinctive facial features, intellectual disability, skeletal abnormalities, short stature, and dermatological disorders, among other clinical manifestations. There is an increased risk of associated autoimmune diseases (such as thrombocytopenic purpura, hemolytic anemia, vitiligo, and type 1 diabetes). Type 1 diabetes is caused by autoimmune destruction of the beta cells of the pancreas and is the most common form of diabetes in children and adolescents. We present three pediatric patients with a diagnosis of Kabuki syndrome and type 1 diabetes, two of whom have an associated second autoimmune disease.

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Publication Details

Journal
Archivos Argentinos de Pediatria
Published
2024-10-28
DOI
https://doi.org/10.5546/aap.2024-10378.eng
Primary Topic
Genomics and Rare Diseases
Type
article
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article

Kabuki syndrome associated with type 1 diabetes mellitus: report of three cases

Nuria Grimberg, Eleazara Rubio Martín, María E Andrés, Yolanda Torres Domínguez et al.
Archivos Argentinos de Pediatria
Genomics and Rare Diseases
article

Kabuki syndrome associated with type 1 diabetes mellitus: report of three cases

Nuria Grimberg, Eleazara Rubio Martín, María E Andrés, Yolanda Torres Domínguez, Malena Silberkasten
article en

Abstract

Kabuki syndrome is a rare genetic disorder characterized by distinctive facial features, intellectual disability, skeletal abnormalities, short stature, and dermatological disorders, among other clinical manifestations. There is an increased risk of associated autoimmune diseases (such as thrombocytopenic purpura, hemolytic anemia, vitiligo, and type 1 diabetes). Type 1 diabetes is caused by autoimmune destruction of the beta cells of the pancreas and is the most common form of diabetes in children and adolescents. We present three pediatric patients with a diagnosis of Kabuki syndrome and type 1 diabetes, two of whom have an associated second autoimmune disease.

Archivos Argentinos de PediatriaVol. 123(3)
Hospital Pedro de Elizalde (AR)
Openalex Percentile: Top 78%
Genomics and Rare Diseases
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