Orofaciodigital syndrome type II (Mohr syndrome): a case report
| Autor: | Ramin Zargarbashi, Fardis Vosoughi, Bita Malekianzadeh |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
medicine.medical_specialty
Pediatrics lcsh:Diseases of the musculoskeletal system media_common.quotation_subject Case Report Orofacial-digital syndrome Iran Oral cavity Fingers 03 medical and health sciences 0302 clinical medicine Rheumatology medicine Humans Family Orthopedics and Sports Medicine Orofaciodigital syndrome 030212 general & internal medicine Girl Child Central incisors media_common Mohr syndrome Polydactyly Syndrome type business.industry Genetic disorder Orofaciodigital Syndromes medicine.disease Child Preschool Orthopedic surgery Female lcsh:RC925-935 business 030217 neurology & neurosurgery |
| Zdroj: | BMC Musculoskeletal Disorders BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-5 (2020) |
| ISSN: | 1471-2474 |
| DOI: | 10.1186/s12891-020-03825-x |
| Popis: | Background Orofacial digital syndrome is a rare genetic disorder with oral cavity, facial and digits anomalies. Orofacial digital syndrome type II, also called the “Mohr syndrome” is a very rare subtype that has been reported scarcely in Asia especially in Japanese patients. Case presentation The case is an Iranian 5-year old girl who had been admitted for orthopedic surgery. She surprisingly had pre and postaxial polydactyly of all the four limbs concurrent with syndromic face and most of the features of Orofaciodigital syndrome type II. Conclusion Mohr syndrome, anesthesia and surgical considerations are discussed in this case report. It is recommended to consider these considerations and the possibility of OFDS in every child with pre and postaxial polydactyly of the four limbs and to try to distinguish type II from other types of ODFS. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink