Your browser doesn't support javascript.
loading
Transient Neonatal Diabetes Mellitus with an Unknown Cause in a 1-Month-Old Infant: A Case Report.
Tarasiewicz, Mateusz; Pietrzykowska, Anna; Wlodarczyk, Julia; Seget, Sebastian; Gadzalska, Karolina; Jakiel, Paulina; Skoczylas, Sebastian; Jarosz-Chobot, Przemyslawa; Borowiec, Maciej.
Afiliação
  • Tarasiewicz M; Department of Children's Diabetology and Pediatrics, Medical University of Silesia, 40-055 Katowice, Poland.
  • Pietrzykowska A; Department of Children's Diabetology and Pediatrics, Medical University of Silesia, 40-055 Katowice, Poland.
  • Wlodarczyk J; Department of Children's Diabetology and Pediatrics, Medical University of Silesia, 40-055 Katowice, Poland.
  • Seget S; Department of Children's Diabetology and Pediatrics, Medical University of Silesia, 40-055 Katowice, Poland.
  • Gadzalska K; Department of Clinical Genetics, Medical University of Lodz, 90-419 Lodz, Poland.
  • Jakiel P; Department of Clinical Genetics, Medical University of Lodz, 90-419 Lodz, Poland.
  • Skoczylas S; Department of Clinical Genetics, Medical University of Lodz, 90-419 Lodz, Poland.
  • Jarosz-Chobot P; Department of Children's Diabetology and Pediatrics, Medical University of Silesia, 40-055 Katowice, Poland.
  • Borowiec M; Department of Clinical Genetics, Medical University of Lodz, 90-419 Lodz, Poland.
Healthcare (Basel) ; 12(13)2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38998792
ABSTRACT
Transient neonatal diabetes mellitus (TNDM) is a genetically heterogeneous form of neonatal diabetes characterized by hyperglycemia that remits during infancy with a tendency to recur in later life. This case report presents the history of a male infant with transient neonatal diabetes mellitus. The patient was treated with a continuous subcutaneous insulin infusion (CSII) and a continuous glucose monitoring (CGM) system until the age of 2 months, when the normoglycemia connected with a withdrawal of treatment was noted. The genetic test results excluded the majority of known mutations related to TNDM. This case report focuses on various genetic mutations and the clinical features connected with them that cause TNDM and highlights the difficulties in the diagnostic and therapeutic processes of this disease. CSII and CGM systems seem to be a safe and effective treatment option in TNDM and may be used in the therapy.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Healthcare (Basel) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Healthcare (Basel) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Polônia