TY  - JOUR
TI  - Michels Syndrome: A Case Report from Turkey and Review of Literature
AB  - 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.
AU  - doğan, murat
AU  - sahin, mustafa
AU  - KARATEPE HASHAS, ARZU SEYHAN
AU  - Hıra, İbrahim
AU  - Erdogan, Murat
DO  - 10.5336/caserep.2017-58417
PY  - 2018
JO  - Türkiye Klinikleri Journal of Case Reports
VL  - 26
IS  - 3
SN  - 2147-9291
SP  - 117
EP  - 121
DB  - TRDizin
UR  - http://search/yayin/detay/356754
ER  -