Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report

Mehmet Şükrü Şahin; Tarkan Ergün

doi:10.2399/emd.12.21931

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Case Report
Online Published: 03 Jul 2014

Hand Microsurg. 2012; 1(3): 103-106

doi: 10.2399/emd.12.21931

Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report

Mehmet Şükrü Şahin, Tarkan Ergün.

Abstract
The congenital constriction band syndrome of lower extremity is a very uncommon and well-described disease which includes several congenital deformities. The true incidence in general population is unknown. The type of malformation depends on the time of gestational period. Although congenital constriction band syndrome is a well-known congenital condition, the development mechanism of this anomaly has not been clarified fully. There are many intrinsic and extrinsic theories regarding the etiology of this rare syndrome. Generally accepted mechanism is the process that consists of the early amniotic rupture leading to formation of mesodermal fibrous strands which constrict and amputate distal portions of limbs. It is characterized by syndactyly, hypoplasia, brachydactyly, symphalangism, symbrachydactyly, club foot, cleft lip, cleft palate, and cranial defects. The lesion can involve skin only or goes to deeper structure up to bone, which can lead to gangrene of foot or autoamputation. The treatment should be tailored to the individual patient. The aim of surgical treatment requires release of deep as well as superficial structures. We are presenting a patient with constriction band syndrome which has been treated because of late onset beginning of entrapment neuropathy at his left leg. To our knowledge, no such cases have been previously reported in the literature.

Key words: Amniotic band, congenital constriction band syndrome, deformity, entrapment, neuropathy

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How to Cite this Article

Pubmed Style

Mehmet Şukru Şahin, Tarkan Ergun. Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand Microsurg. 2012; 1(3): 103-106. doi:10.2399/emd.12.21931

Web Style

Mehmet Şukru Şahin, Tarkan Ergun. Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. https://handmicrosurgeryjournal.com/?mno=163471 [Access: September 12, 2024]. doi:10.2399/emd.12.21931

AMA (American Medical Association) Style

Mehmet Şukru Şahin, Tarkan Ergun. Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand Microsurg. 2012; 1(3): 103-106. doi:10.2399/emd.12.21931

Vancouver/ICMJE Style

Mehmet Şukru Şahin, Tarkan Ergun. Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand Microsurg. (2012), [cited September 12, 2024]; 1(3): 103-106. doi:10.2399/emd.12.21931

Harvard Style

Mehmet Şukru Şahin, Tarkan Ergun (2012) Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand Microsurg, 1 (3), 103-106. doi:10.2399/emd.12.21931

Turabian Style

Mehmet Şukru Şahin, Tarkan Ergun. 2012. Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand and Microsurgery, 1 (3), 103-106. doi:10.2399/emd.12.21931

Chicago Style

Mehmet Şukru Şahin, Tarkan Ergun. "Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report." Hand and Microsurgery 1 (2012), 103-106. doi:10.2399/emd.12.21931

MLA (The Modern Language Association) Style

APA (American Psychological Association) Style

Mehmet Şukru Şahin, Tarkan Ergun (2012) Congenital constriction band syndrome associated with late-onset entrapment neuropathy at distal 1/3 of left crus: a case report. Hand and Microsurgery, 1 (3), 103-106. doi:10.2399/emd.12.21931

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