Autoimmune polyglandular syndrome type 2: A rare condition in childhood

JCRPE Journal of Clinical Research in Pediatric Endocrinology

Volumn 7, Issue 1, 2015, Pages 80-82

  Kirmizibekmez, Heves ^a   Mutlu, Rahime Gül Yeşiltepe ^a   Urganci, Nafiye Demirkiran ^b   Öner, Ayşe ^c  

^a Zeynep Kamil Education and Research Hospital   (Turkey)

^b SISLI ETFAL TRAINING AND RESEARCH HOSPITAL   (Turkey)

^c Academic Hospital   (Turkey)

Author keywords

Autoimmune; Children; Management; Polyendocrinopathy

Indexed keywords

CORTICOTROPIN; ENDOMYSIUM ANTIBODY; FLUDROCORTISONE; GLIADIN ANTIBODY; GLUCOCORTICOID; GLUTAMATE DEHYDROGENASE; HYDROCORTISONE; LEVOTHYROXINE; MINERALOCORTICOID; PANCREAS ISLET CELL ANTIBODY; THYROID ANTIBODY; THYROTROPIN;

ADDISON DISEASE; ADRENAL INSUFFICIENCY; ANOREXIA; ARTICLE; AUTOIMMUNE DISEASE; AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE 2; AUTOIMMUNE THYROIDITIS; AUTOIMMUNITY; CASE REPORT; CELIAC DISEASE; CELL PROLIFERATION; CHILD; CHILDHOOD DISEASE; CRYPT CELL; DETERIORATION; DISTRESS SYNDROME; ECHOGRAPHY; ELECTROLYTE DISTURBANCE; ENDOSCOPIC BIOPSY; FATIGUE; FOLLOW UP; GUILT; HASHIMOTO DISEASE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; INTESTINE VILLUS ATROPHY; LYMPHOCYTIC INFILTRATION; MALE; ORAL GLUCOSE TOLERANCE TEST; PANCREAS ISLET CELL; SCHOOL CHILD; WEIGHT REDUCTION; PATHOLOGY; POLYENDOCRINOPATHY; PROGNOSIS; PSYCHOLOGY;

ADDISON DISEASE; CHILD; DIABETES MELLITUS, TYPE 1; HASHIMOTO DISEASE; HUMANS; MALE; POLYENDOCRINOPATHIES, AUTOIMMUNE; PROGNOSIS;

EID: 84925427614     PISSN: 13085727     EISSN: 13085735     Source Type: Journal    
DOI: 10.4274/jcrpe.1394     Document Type: Article

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