Congenital Constriction Band Syndrome: Clinical Study of Three Cases in Togo

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Congenital Constriction Band Syndrome: Clinical Study of Three Cases in Togo

Authors
  • Foli Agbeko1, 2
  • Fidèle Comlan Dossou3
  • Mawouto Fiawoo1, 4
  • Elom Ounoo Takassi1, 4
  • Mawulolo Kossi Kato4
  • Mawuse Koffi Guédénon1, 4
  • Kokou Agbékogni Réné Segbedji5, 6
  • Djatougbé Ayaovi Elie Akolly1, 4
  • Magnoulelem N’Zonou7
  • Sollim Talboussouma6
  • Mazama Pakoudjare2
  • Homba Daké Batalia3
  • Kokouvi Evenyo Abalo3
  • Edem Koffi Djadou1, 3
  • Kokou Nadiedjoa Douti1, 2
  • Adama Dodji Gbadoe1, 7
  • Yawo Dzayissé Atakouma1, 4
  • Didier Koffi Gnamey1, 4
Type
Published Article
Journal
Asploro Journal of Biomedical and Clinical Case Reports
Publisher
Asploro Open Access Publications
Publication Date
Oct 16, 2021
Accepted Date
Oct 16, 2022
Volume
4
Issue
3
Pages
170–178
Identifiers
DOI: 10.36502/2021/ASJBCCR.6250
Source
MyScienceWork
Keywords
License
Green

Abstract

Introduction: Congenital constriction band syndrome (CCBS) or amniotic band syndrome is a complex set of congenital malformations, mainly affecting the limbs, but also the craniofacial and thoraco-abdominal region. The Patients: The purpose of this work is to describe the clinical and diagnostic aspects of CCBS in Togo in relation to 03 clinical cases. The Primary Diagnoses, Interventions, and Outcomes: The first case is characterized by an asymmetric bilateral superficial constriction groove of the lower limbs, pseudosyndactylias and synostosis of the tibia and fibula on X-ray. The second has a deep strangulation in the left arm with an amputation of the fingers associated with hypochromic skin lesions, poorly hemmed polylobal ear and skin growths. The latter characterized by persistent bridle, strangulation and ischemia downstream of that of the left wrist with postnatal amputation of the left hand. Conclusion: The strengthening of antenatal diagnosis, the introduction of genetic counselling and the establishment of a national malformations register should make it possible to improve the management of cases of amniotic flange disease.

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