مرکز منطقه ای اطلاع رساني علوم و فناوري - Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22

Title of article :

Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22

Author/Authors :

Mosallanejad، Asieh نويسنده Imam Hossein Medical Center, Shahid Beheshti University of Medical Science, Tehran, Iran. Mosallanejad, Asieh , Sayarifard، Fatemeh نويسنده Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran. Sayarifard, Fatemeh , Hosseinverdi، Sima نويسنده Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Hosseinverdi, Sima , Abbasi، Farzaneh نويسنده Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran. Abbasi, Farzaneh , Shabni Mirzaee، Hosein نويسنده Department of Pediatric Endocrinology, Bahrami Hospital, Tehran University of Medical Sciences,Tehran, Iran. Shabni Mirzaee, Hosein , Rezaei، Nima نويسنده ,

Issue Information :

ماهنامه با شماره پیاپی 0 سال 2015

Pages :

From page :

782

To page :

784

Abstract :

There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma. The result of karyotype showed 47XX, with extra marker chromosome 22. Although such a manifestation had not been reported in the literature, it should be considered as a very rare manifestation of the disease.

Journal title :

Acta Medica Iranica

Serial Year :

2015

Journal title :

Acta Medica Iranica

Record number :

2385313

Link To Document :

https://search.isc.ac/dl/search/defaultta.aspx?DTC=10&DC=2385313