Michels Syndrome: A Case Report from Turkey and Review of Literature
Yıl: 2018 Cilt: 26 Sayı: 3 Sayfa Aralığı: 117 - 121 Metin Dili: İngilizce DOI: 10.5336/caserep.2017-58417 İndeks Tarihi: 14-09-2020
Michels Syndrome: A Case Report from Turkey and Review of Literature
Öz: A 4-year and 7 month-old boy was admitted to our facility with the complaints of blepharophimosis, blepharoptosis, and epicanthus inversus in association with hypertelorism, cleftpalate, mental deficiency, hearing loss, and craniosynostosis. The patient also had umbilical depression and small hands with bilaterally short fifth fingers. These clinical features led us to thinkthat they are the components of a single syndrome, which may be referred to as “3MC1 syndrome.”The main characteristics of 3MC1 syndrome are the facial dysmorphic traits and include hypertelorism, blepharophimosis and blepharoptosis. Other related symptoms are cleft lip and palate,postnatal growth deficit, cognitive impairment and hearing loss, craniocynosis, radioulnar synostosis and genital and vesicorenal anomalies. The etiological causes of 3MC1 are still unknown.
Anahtar Kelime: Belge Türü: Makale Makale Türü: Araştırma Makalesi Erişim Türü: Erişime Açık
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| APA | doğan m, Hıra İ, sahin m, Erdogan M, KARATEPE HASHAS A (2018). Michels Syndrome: A Case Report from Turkey and Review of Literature. , 117 - 121. 10.5336/caserep.2017-58417 |
| Chicago | doğan murat,Hıra İbrahim,sahin mustafa,Erdogan Murat,KARATEPE HASHAS ARZU SEYHAN Michels Syndrome: A Case Report from Turkey and Review of Literature. (2018): 117 - 121. 10.5336/caserep.2017-58417 |
| MLA | doğan murat,Hıra İbrahim,sahin mustafa,Erdogan Murat,KARATEPE HASHAS ARZU SEYHAN Michels Syndrome: A Case Report from Turkey and Review of Literature. , 2018, ss.117 - 121. 10.5336/caserep.2017-58417 |
| AMA | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A Michels Syndrome: A Case Report from Turkey and Review of Literature. . 2018; 117 - 121. 10.5336/caserep.2017-58417 |
| Vancouver | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A Michels Syndrome: A Case Report from Turkey and Review of Literature. . 2018; 117 - 121. 10.5336/caserep.2017-58417 |
| IEEE | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A "Michels Syndrome: A Case Report from Turkey and Review of Literature." , ss.117 - 121, 2018. 10.5336/caserep.2017-58417 |
| ISNAD | doğan, murat vd. "Michels Syndrome: A Case Report from Turkey and Review of Literature". (2018), 117-121. https://doi.org/10.5336/caserep.2017-58417 |
| APA | doğan m, Hıra İ, sahin m, Erdogan M, KARATEPE HASHAS A (2018). Michels Syndrome: A Case Report from Turkey and Review of Literature. Türkiye Klinikleri Journal of Case Reports, 26(3), 117 - 121. 10.5336/caserep.2017-58417 |
| Chicago | doğan murat,Hıra İbrahim,sahin mustafa,Erdogan Murat,KARATEPE HASHAS ARZU SEYHAN Michels Syndrome: A Case Report from Turkey and Review of Literature. Türkiye Klinikleri Journal of Case Reports 26, no.3 (2018): 117 - 121. 10.5336/caserep.2017-58417 |
| MLA | doğan murat,Hıra İbrahim,sahin mustafa,Erdogan Murat,KARATEPE HASHAS ARZU SEYHAN Michels Syndrome: A Case Report from Turkey and Review of Literature. Türkiye Klinikleri Journal of Case Reports, vol.26, no.3, 2018, ss.117 - 121. 10.5336/caserep.2017-58417 |
| AMA | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A Michels Syndrome: A Case Report from Turkey and Review of Literature. Türkiye Klinikleri Journal of Case Reports. 2018; 26(3): 117 - 121. 10.5336/caserep.2017-58417 |
| Vancouver | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A Michels Syndrome: A Case Report from Turkey and Review of Literature. Türkiye Klinikleri Journal of Case Reports. 2018; 26(3): 117 - 121. 10.5336/caserep.2017-58417 |
| IEEE | doğan m,Hıra İ,sahin m,Erdogan M,KARATEPE HASHAS A "Michels Syndrome: A Case Report from Turkey and Review of Literature." Türkiye Klinikleri Journal of Case Reports, 26, ss.117 - 121, 2018. 10.5336/caserep.2017-58417 |
| ISNAD | doğan, murat vd. "Michels Syndrome: A Case Report from Turkey and Review of Literature". Türkiye Klinikleri Journal of Case Reports 26/3 (2018), 117-121. https://doi.org/10.5336/caserep.2017-58417 |
