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...
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| Format: | Article |
| Language: | fas |
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University of Social Welfare and Rehabilitation Sciences
2006-01-01
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| Series: | Journal of Rehabilitation |
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| Online Access: | http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-73&slc_lang=en&sid=1 |
| _version_ | 1818128975654813696 |
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| author | Yousef Shafaghati Ghazal Vakili Javad Jannati |
| author_facet | Yousef Shafaghati Ghazal Vakili Javad Jannati |
| author_sort | Yousef Shafaghati |
| collection | DOAJ |
| description | 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. clinical symptoms are obvious enough and experienced teachers can easily diagnose the disease. In this care report, a 21-year-old Iranian male patient, who showed completely the symptoms of acrodysostosis, is reported. According to our experience, this is the first known case in Iran. There must be other cases in mentally retarded patients who are dysmorphic. Therefore, it is necessary to be aware of symptoms of this disease when facing with dysmorphic mentally retarded patients. |
| first_indexed | 2024-12-11T07:41:47Z |
| format | Article |
| id | doaj.art-512ccdd808a6440dac1ad6a64f3030ef |
| institution | Directory Open Access Journal |
| issn | 1607-2960 1607-2960 |
| language | fas |
| last_indexed | 2024-12-11T07:41:47Z |
| publishDate | 2006-01-01 |
| publisher | University of Social Welfare and Rehabilitation Sciences |
| record_format | Article |
| series | Journal of Rehabilitation |
| spelling | doaj.art-512ccdd808a6440dac1ad6a64f3030ef2022-12-22T01:15:33ZfasUniversity of Social Welfare and Rehabilitation SciencesJournal of Rehabilitation1607-29601607-29602006-01-01644548Case Report: Acrodysostosis: Report of a 21 Years Old Iranian PatientYousef Shafaghati0Ghazal Vakili1Javad Jannati2 University of Welfare & Rehabilitation Siences, Tehran, Iran. 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. clinical symptoms are obvious enough and experienced teachers can easily diagnose the disease. In this care report, a 21-year-old Iranian male patient, who showed completely the symptoms of acrodysostosis, is reported. According to our experience, this is the first known case in Iran. There must be other cases in mentally retarded patients who are dysmorphic. Therefore, it is necessary to be aware of symptoms of this disease when facing with dysmorphic mentally retarded patients.http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-73&slc_lang=en&sid=1Acrodysostosis Maroteaux-malamut syndrome Short matacarps Arkless-Graham syndrome Acrodysplasia Cone-shaped epiphyses Peripheral dysostosis |
| spellingShingle | Yousef Shafaghati Ghazal Vakili Javad Jannati Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient Journal of Rehabilitation Acrodysostosis Maroteaux-malamut syndrome Short matacarps Arkless-Graham syndrome Acrodysplasia Cone-shaped epiphyses Peripheral dysostosis |
| title | Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient |
| title_full | Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient |
| title_fullStr | Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient |
| title_full_unstemmed | Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient |
| title_short | Case Report: Acrodysostosis: Report of a 21 Years Old Iranian Patient |
| title_sort | case report acrodysostosis report of a 21 years old iranian patient |
| topic | Acrodysostosis Maroteaux-malamut syndrome Short matacarps Arkless-Graham syndrome Acrodysplasia Cone-shaped epiphyses Peripheral dysostosis |
| url | http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-73&slc_lang=en&sid=1 |
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