Congenital true complete symphalangism of all proximal interphalangeal joints of hands with carpal anomalies: a case report.

Symphalangism is a rare condition which manifests in either PIP or DIP joint congenital fusion. Symphalangism may be with some other skeletal deformities. In our case, all PIP joints of both hands were fused with bilateral hypoplasia of carpal bones and Minaar type III lunatotriquetral coalition congenitally. No motion was detected in PIP joints with absence of cutaneous creases over all PIP joints. Radiologically, carpal hypoplasia and lunatotriquetral coalition were seen in all fingers with the absence of PIP joints. The patient's skeletal survey revealed no other pathology. He had no complaints related to his hands. So, regular follow-up was recommended. This pathology was presented as rarely observed although clinical problem is usually not so much.

Yazar Tuncay I.
Akpinar F.
Tosun N.
Yayın Türü Article
Tek Biçim Adres https://hdl.handle.net/20.500.12628/4889
Tek Biçim Adres 10.1142/S0218810401000692
Koleksiyonlar Araştırma Çıktıları | WoS | Scopus | TR-Dizin | PubMed | SOBİAD
Scopus İndeksli Yayınlar Koleksiyonu
Dergi Adı Hand surgery : an international journal devoted to hand and upper limb surgery and related research : journal of the Asia-Pacific Federation of Societies for Surgery of the Hand
Dergi Cilt Bilgisi 6
Dergi Sayısı 2
Sayfalar 223 - 226
Yayın Yılı 2001
Eser Adı
[dc.title]
Congenital true complete symphalangism of all proximal interphalangeal joints of hands with carpal anomalies: a case report.
Yazar
[dc.contributor.author]
Tuncay I.
Yazar
[dc.contributor.author]
Akpinar F.
Yazar
[dc.contributor.author]
Tosun N.
Yayın Yılı
[dc.date.issued]
2001
Yayın Türü
[dc.type]
article
Özet
[dc.description.abstract]
Symphalangism is a rare condition which manifests in either PIP or DIP joint congenital fusion. Symphalangism may be with some other skeletal deformities. In our case, all PIP joints of both hands were fused with bilateral hypoplasia of carpal bones and Minaar type III lunatotriquetral coalition congenitally. No motion was detected in PIP joints with absence of cutaneous creases over all PIP joints. Radiologically, carpal hypoplasia and lunatotriquetral coalition were seen in all fingers with the absence of PIP joints. The patient's skeletal survey revealed no other pathology. He had no complaints related to his hands. So, regular follow-up was recommended. This pathology was presented as rarely observed although clinical problem is usually not so much.
Kayıt Giriş Tarihi
[dc.date.accessioned]
2019-12-23
Açık Erişim Tarihi
[dc.date.available]
2019-12-23
Yayın Dili
[dc.language.iso]
eng
Haklar
[dc.rights]
info:eu-repo/semantics/closedAccess
ISSN
[dc.identifier.issn]
0218-8104
İlk Sayfa Sayısı
[dc.identifier.startpage]
223
Son Sayfa Sayısı
[dc.identifier.endpage]
226
Dergi Adı
[dc.relation.journal]
Hand surgery : an international journal devoted to hand and upper limb surgery and related research : journal of the Asia-Pacific Federation of Societies for Surgery of the Hand
Dergi Sayısı
[dc.identifier.issue]
2
Dergi Cilt Bilgisi
[dc.identifier.volume]
6
Tek Biçim Adres
[dc.identifier.uri]
https://dx.doi.org/10.1142/S0218810401000692
Tek Biçim Adres
[dc.identifier.uri]
https://hdl.handle.net/20.500.12628/4889
Görüntülenme Sayısı ( Şehir )
Görüntülenme Sayısı ( Ülke )
Görüntülenme Sayısı ( Zaman Dağılımı )
Görüntülenme
4
09.12.2022 tarihinden bu yana
İndirme
1
09.12.2022 tarihinden bu yana
Son Erişim Tarihi
21 Şubat 2024 22:03
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Tıklayınız
joints lunatotriquetral coalition skeletal carpal hypoplasia absence pathology Symphalangism observed patient survey usually problem revealed clinical although regular rarely complaints presented related recommended follow-up fingers congenitally Radiologically deformities condition manifests either congenital fusion bilateral Minaar
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