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Information Journal Paper

Title

REPORTING THREE CASES OF ROGER'S SYNDROME IN CHILDREN (CASE REPORT)

Pages

  121-127

Abstract

 Roger's syndrome is a rare form of diabetes in children that is characterized with early onset of DIABETES MELLITUS, MEGALOBLASTIC ANEMIA, and SENSORY NEURAL HEARING LOSS. In this report three cases of this syndrome from consanguineous Iranian families are introduced (two siblings and a cousin). They referred to pediatric ward of Imam Reza Hospital with hyperglycemia, anemia and SENSORY NEURAL HEARING LOSS.Molecular genetics study revealed novel mutation in SLC19A2 gene. Thiamin was used in order to treat the patients. Afterwards, anemia was resolved in all patients and normoglycemia achieved in two of the patients, however, hearing loss remained in all three.

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    APA: Copy

    GHAEMI, NOSRAT, VAKILI, RAHIM, ZAMANFAR, DANIEL, ABASZADEGAN, MOHAMMAD REZA, GHAHRAMAN, MARTA, & MOHSENI SARAVI, BENYAMIN. (2012). REPORTING THREE CASES OF ROGER'S SYNDROME IN CHILDREN (CASE REPORT). JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 22(89), 121-127. SID. https://sid.ir/paper/44705/en

    Vancouver: Copy

    GHAEMI NOSRAT, VAKILI RAHIM, ZAMANFAR DANIEL, ABASZADEGAN MOHAMMAD REZA, GHAHRAMAN MARTA, MOHSENI SARAVI BENYAMIN. REPORTING THREE CASES OF ROGER'S SYNDROME IN CHILDREN (CASE REPORT). JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2012;22(89):121-127. Available from: https://sid.ir/paper/44705/en

    IEEE: Copy

    NOSRAT GHAEMI, RAHIM VAKILI, DANIEL ZAMANFAR, MOHAMMAD REZA ABASZADEGAN, MARTA GHAHRAMAN, and BENYAMIN MOHSENI SARAVI, “REPORTING THREE CASES OF ROGER'S SYNDROME IN CHILDREN (CASE REPORT),” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 22, no. 89, pp. 121–127, 2012, [Online]. Available: https://sid.ir/paper/44705/en

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