Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient
Acrodysostosis is a very rare congenital disorder. Less than 80 cases have been reported in the medical literature until now. Most of the reported cases were sporadic, but in some families evidences like father's old age and affected parent and child gives rise to autosomal dominant inheritance...
Main Authors: | Yousef Shafaghati, Ghazal Vakili, Javad Jannati |
---|---|
Format: | Article |
Language: | fas |
Published: |
University of Social Welfare and Rehabilitation Sciences
2006-01-01
|
Series: | Journal of Rehabilitation |
Subjects: | |
Online Access: | http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-73&slc_lang=en&sid=1 |
Similar Items
-
Acrodysostosis: A case report.
by: Dr. Gargi Pathak, et al.
Published: (2018-06-01) -
A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case report
by: Gunda Petraitytė, et al.
Published: (2021-04-01) -
Craniofacial dysostosis and a case report include surgical treatment of a Crouzon syndrome
by: Mahmood Hashemi H.
Published: (1999-07-01) -
A Case Report of Mucopolysaccharidosis Type VI
by: SJ Hosseini, et al.
Published: (2018-12-01) -
Mandibulofacial dysostosis (Treacher Collins syndrome): A case report and review of literature
by: Raj Renju, et al.
Published: (2014-01-01)