Clinical manifestations of a sporadic maturity-onset diabetes of the young (MODY) 5 with a whole deletion of HNF1B based on 17q12 microdeletion

Keyphrases

• 17q12 Microdeletion 100%
• 17q12 Microdeletion Syndrome 66%
• Array Comparative Genomic Hybridization (aCGH) 33%
• Autoimmune Diabetes 33%
• Autoimmune Diabetes Mellitus 33%
• Chromosomal Deletion 33%
• Chromosomal Microarray 33%
• Clinical Characteristics 33%
• Clinical Heterogeneity 33%
• Clinical Manifestations 100%
• Early Onset 33%
• Family History of Diabetes 33%
• Hepatocyte nuclear Factor 100%
• Hyperuricemia 33%
• Hypomagnesemia 33%
• Japanese Workers 33%
• Kidney 33%
• Liver Enzymes 33%
• Maturity-onset Diabetes of the Young 100%
• Maturity-onset Diabetes of the Young type 5 66%
• Multiplex Ligation-dependent Probe Amplification 33%
• Multisystemic 33%
• Old Japanese 33%
• Pancreatic Exocrine Dysfunction 33%
• Pancreatic Hypoplasia 33%
• Serum Levels 33%
• Sporadic Cases 66%
• Systemic Symptoms 33%
• Whole Gene Deletion 33%

Medicine and Dentistry

• Allele 25%
• Array Comparative Genomic Hybridization 25%
• Autoimmune Diabetes 25%
• Chromosome Analysis 25%
• Chromosome Deletion 25%
• Diabetes 25%
• Diabetes Mellitus 25%
• Family History 25%
• Gene Deletion 25%
• Hepatocyte Nuclear Factor 1beta 100%
• Hyperuricemia 25%
• Hypomagnesemia 25%
• Hypoplasia 25%
• Liver Enzyme 25%
• Maturity Onset Diabetes of the Young 100%
• Multiplex Ligation Dependent Probe Amplification 25%
• Solitary Kidney 25%

Biochemistry, Genetics and Molecular Biology

• Allele 33%
• Array Comparative Genomic Hybridization 33%
• Blood Level 33%
• Enzyme 33%
• Gene Deletion 33%
• Hepatocyte Nuclear Factor 1beta 100%
• Hyperuricemia 33%
• Hypomagnesemia 33%
• Microdeletion Syndrome 66%
• Multiplex Ligation-Dependent Probe Amplification 33%