DEND syndrome | About the Disease | GARD DEND syndrome is caused by genetic mutations, also known as pathogenic variants Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing
DEND syndrome - National Organization for Rare Disorders DEND syndrome is a very rare, generally severe form of neonatal diabetes mellitus (NDM) characterized by a triad of developmental delay, epilepsy, and neonatal diabetes
DEND syndrome - Orphanet A rare form of neonatal diabetes mellitus characterized by a triad of Developmental delay, Epilepsy, and Neonatal Diabetes (DEND syndrome), with a generally severe course
Understanding Neonatal Diabetes and DEND Syndrome DEND syndrome is a rare autoimmune disorder that primarily affects the small intestine The major symptoms include abdominal pain and diarrhea, which often resolve with time
Dend Syndrome - MalaCards A rare form of neonatal diabetes mellitus characterized by a triad of Developmental delay, Epilepsy, and Neonatal Diabetes (DEND syndrome), with a generally severe course
DEND syndrome - Global Genes DEND syndrome is a very rare generally severe form of neonatal diabetes mellitus (NDM see this term) characterized by a triad of developmental delay epilepsy and neonatal diabetes
Clinical Signs and Symptoms - Orphanet ORPHA:79134 DEND syndrome The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO)
DEND syndrome - NIH Genetic Testing Registry (GTR) - NCBI DEND syndrome represents the most severe end of the neonatal diabetes mellitus spectrum The associated neurologic features range from mild psychomotor retardation to severe developmental delay
Permanent Neonatal Diabetes (DEND Syndrome) - PubMed DEND syndrome is a very rare syndrome of permanent neonatal diabetes mellitus, with an incidence of < 1 1000,000 It is defined as a triad of developmental delay, epilepsy, and neonatal diabetes