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

Author:

Agbeko Foli1ORCID,Dossou Fidèle Comlan2,Fiawoo Mawouto3,Takassi Elom Ounoo3,Kato Mawulolo Kossi4,Guédénon Mawuse Koffi3,Segbedji Kokou Agbékogni Réné5,Akolly Djatougbé Ayaovi Elie3,N’Zonou Magnoulelem6,Talboussouma Sollim7,Pakoudjare Mazama8,Batalia Homba Daké2,Abalo Kokouvi Evenyo2,Djadou Edem Koffi9,Douti Kokou Nadiedjoa1,Gbadoe Adama Dodji10,Atakouma Yawo Dzayissé3,Gnamey Didier Koffi3

Affiliation:

1. Département de Pédiatrie / Faculté des Sciences de la Santé, Université de Lomé, Lomé, Togo; CHU Campus, Service de Pédiatrie, Lomé, Togo

2. CHR Sokodé, Service de Pédiatrie, Sokodé, Togo

3. Département de Pédiatrie / Faculté des Sciences de la Santé, Université de Lomé, Lomé, Togo; CHU Sylvanus Olympio, Service de Pédiatrie, Lomé, Togo

4. CHU Sylvanus Olympio, Service de Pédiatrie, Lomé, Togo

5. Département de Pédiatrie / Faculté des Sciences de la Santé, Université de Kara, Kara, Togo; CHU Kara, Service de Pédiatrie, Kara, Togo

6. Hôpital de Bè, Service de Pédiatrie, Lomé, Togo

7. CHU Kara, Service de Pédiatrie, Kara, Togo

8. CHU Campus, Service de Pédiatrie, Lomé, Togo

9. Département de Pédiatrie / Faculté des Sciences de la Santé, Université de Lomé, Lomé, Togo; CHR Sokodé, Service de Pédiatrie, Sokodé, Togo

10. Département de Pédiatrie / Faculté des Sciences de la Santé, Université de Lomé, Lomé, Togo; Hôpital de Bè, Service de Pédiatrie, Lomé, Togo

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.

Publisher

Asploro Open Access Publications

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