Maternally inherited diabetes and deafness (MIDD): Diagnosis and management

Journal of Diabetes and its Complications

Volumn 28, Issue 4, 2014, Pages 542-546

  Naing, Aye ^a   Kenchaiah, Manohar ^a   Krishnan, Binu ^a   Mir, Farheen ^b   Charnley, Amanda ^a   Egan, Catherine ^c   Bano, Gul ^d  

^a ST GEORGE S HOSPITAL   (United Kingdom)

^b PRINCESS ALEXANDRA HOSPITAL   (United Kingdom)

^c MOORFIELDS EYE HOSPITAL   (United Kingdom)

^d ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

A to G substitution at position 3243; Coenzyme Q10; Deafness; Familial diabetes; Mitochondrial disease; Mitochondrial DNA; Mutation 3243 in mitochondrial diabetes; Retinal dystrophy

Indexed keywords

AUTOANTIBODY; GLUTAMATE DECARBOXYLASE; MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; FAMILY HISTORY; FEMALE; FOLLOW UP; HUMAN; MALE; MATERNALLY INHERITED DIABETES AND DEAFNESS; MIDDLE AGED; MITOCHONDRIAL DNA DISORDER; NON INSULIN DEPENDENT DIABETES MELLITUS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RESTLESS LEGS SYNDROME; RETINA DYSTROPHY; TREATMENT INDICATION; UNSTEADY GAIT; AMINO ACID SUBSTITUTION; CASE REPORT; COMPLICATION; DEAFNESS; DIABETES MELLITUS, TYPE 2; DIABETIC RETINOPATHY; DIAGNOSTIC ERROR; DIFFERENTIAL DIAGNOSIS; FAMILY HEALTH; GENETICS; MACULAR DEGENERATION; PATHOPHYSIOLOGY; PEDIGREE; POINT MUTATION; SEVERITY OF ILLNESS INDEX; UNITED KINGDOM;

AGED; AMINO ACID SUBSTITUTION; DEAFNESS; DIABETES MELLITUS, TYPE 2; DIABETIC RETINOPATHY; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC ERRORS; DNA, MITOCHONDRIAL; ENGLAND; FAMILY HEALTH; FEMALE; HUMANS; MACULAR DEGENERATION; PEDIGREE; POINT MUTATION; SEVERITY OF ILLNESS INDEX;

EID: 84903317449     PISSN: 10568727     EISSN: 1873460X     Source Type: Journal    
DOI: 10.1016/j.jdiacomp.2014.03.006     Document Type: Article

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