CONGENITAL ARHINIA: A RARE CASE REPORT

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HASHEMIAN NEJAD NASRIN; HOSEINI BIBI LEILA

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Journal Paper

Paper Information

Journal: Journal of Sabzevar University of Medical Sciences Year:2014 | Volume:20 | Issue:5 (SPECIAL) Page(s): 643-647

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Information Journal Paper

Title

CONGENITAL ARHINIA: A RARE CASE REPORT

Author(s)

HASHEMIAN NEJAD NASRIN | HOSEINI BIBI LEILA | Issue Writer Certificate

Keywords

CONGENITAL ARHINIAQ2

HYPERTELORISMQ2

CASE REPORTQ2

Abstract

Introduction: CONGENITAL ARHINIA is a very rare anomalia which can be observed total or partial arhinia. We assessed a case which is affected to CONGENITAL ARHINIA, its reasons and signs in the present study.Case report: The patient is a 41w neonate who is affected to CONGENITAL ARHINIA, HYPERTELORISM, cleft lip and palate. There was just a significant note in neonatal history of family which showed their first child was affected to anomalia. The neonate was transferred to a well-equip center for doing more assessments. At the present time, general condition of the neonate is good.Conclusion: CONGENITAL ARHINIA is a very rare anomaly with an unknown etiology. This anomaly may be associated with the other medline anomalies.

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APA: Copy

HASHEMIAN NEJAD, NASRIN, & HOSEINI, BIBI LEILA. (2014). CONGENITAL ARHINIA: A RARE CASE REPORT. JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES, 20(5 (SPECIAL)), 643-647. SID. https://sid.ir/paper/82027/en

Vancouver: Copy

HASHEMIAN NEJAD NASRIN, HOSEINI BIBI LEILA. CONGENITAL ARHINIA: A RARE CASE REPORT. JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2014;20(5 (SPECIAL)):643-647. Available from: https://sid.ir/paper/82027/en

IEEE: Copy

NASRIN HASHEMIAN NEJAD, and BIBI LEILA HOSEINI, “CONGENITAL ARHINIA: A RARE CASE REPORT,” JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES, vol. 20, no. 5 (SPECIAL), pp. 643–647, 2014, [Online]. Available: https://sid.ir/paper/82027/en

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