JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2011; 21 (3): 187-189
Dans Anglais
| IMEMR
| ID: emr-129573
ABSTRACT
Eight years old girl presented with mucocutaneous candidiasis, nail dystrophy, twitching left half of face, progressively increasing generalized skin hyperpigmentation and hypopigmented patches over both shins. Her investigations revealed low intact PTH level, low serum cortisol, high ACTH, impaired glucose tolerance test and candidal onycomycosis. She was diagnosed as Polyglandular Autoimmune Syndrome [PGA] type I. She also developed idiopathic generalized epileptiform seizures and Alcaligenes faecalis septicemia not previously reported with PGA type I. The patient responded well to alphacalcidol, hydrocortisone, valproate sodium, topical antifungal and systemic antibiotic
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Indice:
Méditerranée orientale
Sujet Principal:
Crises épileptiques
/
Maladies auto-immunes
/
Sepsie
/
Alcaligenes faecalis
/
Hypocalcémie
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Femelle
/
Humains
langue:
Anglais
Texte intégral:
J. Coll. Physicians Surg. Pak.
Année:
2011
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