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Information Journal Paper

Title

A Patient with Trisomy 4p and Monosomy 10q (Case Report)

Pages

  414-417

Abstract

 Translocations are the most common structural abnormality in the human genome. Carriers of balanced chromosome rearrangements exhibit increased risk of abortion or a chromosomally-unbalanced child. The present study was carried out in 2017 at the Iranian Blood Transfusion Research Center. This study reported a rare chromosomal disorder with 4p duplication and 10q distal deletion syndrome which is associated with various complications at birth. Defects included the following characteristics: dysmorphic facial characteristic, hand or foot anomalies, growth retardation, developmental delay, strabismus, heart defects and renal anomalies. Cytogenetic analysis and Array CGH were performed and, for the first time, we reported a patient with trisomy 4p16. 3p12 and monosomy 10q26. 3. The patient was found to have: arr 4p16. 3p12 (37, 152– 45, 490, 207) x3, 10q26. 3 (134, 872, 562– 135, 434, 149) x1 genomic imbalances.

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  • Cite

    APA: Copy

    SOBHANI, MARYAM, TAHMASEBI, PARISA, NASIRI, FATEMEH, Rahnama, Mitra, KARIMINEJAD, ROXANA, & TABATABAIEFAR, MOHAMMAD AMIN. (2019). A Patient with Trisomy 4p and Monosomy 10q (Case Report). ARCHIVES OF IRANIAN MEDICINE, 22(7), 414-417. SID. https://sid.ir/paper/281847/en

    Vancouver: Copy

    SOBHANI MARYAM, TAHMASEBI PARISA, NASIRI FATEMEH, Rahnama Mitra, KARIMINEJAD ROXANA, TABATABAIEFAR MOHAMMAD AMIN. A Patient with Trisomy 4p and Monosomy 10q (Case Report). ARCHIVES OF IRANIAN MEDICINE[Internet]. 2019;22(7):414-417. Available from: https://sid.ir/paper/281847/en

    IEEE: Copy

    MARYAM SOBHANI, PARISA TAHMASEBI, FATEMEH NASIRI, Mitra Rahnama, ROXANA KARIMINEJAD, and MOHAMMAD AMIN TABATABAIEFAR, “A Patient with Trisomy 4p and Monosomy 10q (Case Report),” ARCHIVES OF IRANIAN MEDICINE, vol. 22, no. 7, pp. 414–417, 2019, [Online]. Available: https://sid.ir/paper/281847/en

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