Permanent neonatal diabetes due to KCNJ11 gene mutation.

Letha, S; Mammen, Darly; Valamparampil, Joseph J

Letha, S; Mammen, Darly; Valamparampil, Joseph J.

Affiliation

Letha S; Department of Pediatrics, Government Medical College, Kottayam, Kerala, India. drletha@gmail.com

Indian J Pediatr ; 74(10): 947-9, 2007 Oct.

Article in En | MEDLINE | ID: mdl-17978456

Subject(s)

DNA Mutational Analysis; Diabetes Mellitus, Type 1/genetics; Potassium Channels, Inwardly Rectifying/genetics; Acute Kidney Injury/blood; Acute Kidney Injury/diagnosis; Amino Acid Substitution/genetics; Arginine/genetics; Blood Glucose/metabolism; Cysteine/genetics; Diabetes Mellitus, Type 1/diagnosis; Diabetes Mellitus, Type 1/drug therapy; Diabetic Ketoacidosis/blood; Diabetic Ketoacidosis/diagnosis; Diabetic Ketoacidosis/drug therapy; Diabetic Ketoacidosis/genetics; Female; Genetic Carrier Screening; Glyburide/administration & dosage; Humans; Hypoglycemic Agents/administration & dosage; Infant; Infant, Newborn; Insulin/administration & dosage; Insulin/blood

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Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Potassium Channels, Inwardly Rectifying / Diabetes Mellitus, Type 1 Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Newborn Language: En Journal: Indian J Pediatr Year: 2007 Document type: Article Affiliation country: India

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