Publications by authors named "T Inukai"

Article Synopsis
  • CHDED (Congenital Heart Defect and Ectodermal Dysplasia) is an autosomal dominant disorder linked to the PRKD1 gene, characterized by heart issues and ectodermal abnormalities.
  • A case study of a 9-month-old Japanese girl demonstrated brain calcifications and seizures, revealing a new pathogenic variant in the PRKD1 gene.
  • It is suggested that PRKD1, along with ITGB2 and JAM2, may interact through a common signaling pathway leading to brain calcifications, providing insight into the genetic basis of this disorder.
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Purpose: The JCCG ALL-B12 clinical trial aimed to evaluate the effectiveness of unvalidated treatment phases for pediatric ALL and develop a safety-focused treatment framework.

Patients And Methods: Patients age 1-19 years with newly diagnosed B-ALL were enrolled in this study. These patients were stratified into standard-risk (SR), intermediate-risk (IR), and high-risk (HR) groups.

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Aims The main purpose of this study was to evaluate the associations between circulating angiopoietin-like protein 6 (ANGPTL6) levels and various diabetes- and atherosclerosis-related variables in patients with type 2 diabetes. Methods Serum ANGPTL6 levels in patients with type 2 diabetes hospitalized for glycemic control and/or diabetic education were measured using a chemiluminescent immunoassay (CLIA). Results Most patients had elevated HbA1c levels; 85.

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Summary: Maturity-onset diabetes of the young (MODY) is a group of monogenic forms of diabetes mellitus characterized by early-onset diabetes with dominant inheritance of beta-cell dysfunction. There are few reports of the coinheritance of glucokinase (GCK) and hepatocyte nuclear factor 1 alpha gene (HNF1A) variants underlying MODY in patients. Herein, we describe a case involving combinations of monoallelic GCK and HNF1A variants associated with MODY.

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