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Results 1 - 7 of 7 for familial hyperinsulinism
  1. HADH gene 
    ... reported in a small number of people with familial hyperinsulinism. This disorder is characterized by abnormally high levels ... at least five HADH gene mutations that cause familial hyperinsulinism. These mutations severely reduce 3-hydroxyacyl-CoA dehydrogenase ...
    https://medlineplus.gov/genetics/gene/hadh - Genetics
  2. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... dehydrogenase deficiency Familial dysautonomia Congenital hyperinsulinism , also called familial hyperinsulinism Familial Mediterranean fever Fanconi anemia GRACILE syndrome Gaucher ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  3. Congenital hyperinsulinism 
    ... Testing Registry: Exercise-induced hyperinsulinism Genetic Testing Registry: Familial hyperinsulinism Genetic Testing Registry: Hyperinsulinemic hypoglycemia, familial, 2 Genetic ...
    https://medlineplus.gov/.../condition/congenital-hyperinsulinism - Genetics
  4. ABCC8 gene 
    The ABCC8 gene provides instructions for making the sulfonylurea receptor 1 (SUR1) protein. The SUR1 protein is one part (subunit) of the ATP-sensitive potassium ( ...
    https://medlineplus.gov/genetics/gene/abcc8 - Genetics
  5. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... glucose (hypoglycemia), and abnormally high levels of insulin (hyperinsulinism). Insulin controls the amount of glucose that moves ... Testing Registry: Deficiency of 3-hydroxyacyl-CoA dehydrogenase Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  6. GCK gene 
    ... Health Condition MedlinePlus Genetics provides information about Congenital hyperinsulinism More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/gck - Genetics
  7. Permanent neonatal diabetes mellitus 
    ... sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism. Hum Mutat. 2009 Feb;30(2):170-80. ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics