FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report

FATCO syndrome (Fibular aplasia, tibial campomelia, and oligosyndactyly ) is a very rare malformation of an unknown genetic basis. It more commonly occurs in male children, and the lower extremities are more frequently affected. This is a case of a male newborn with the rare FATCO syndrome. It is th...

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Main Authors: Almir Kajevic, Haris Plojovic, Dzemail Smail Detanac, Suada Malicevic, Azra Kajevic, Dzenana Avdo Detanac, Mirza Corovic
Format: Article
Language:English
Published: Slovenian Medical Association 2024-12-01
Series:Zdravniški Vestnik
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Online Access:https://vestnik.szd.si/index.php/ZdravVest/article/view/3531
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author Almir Kajevic
Haris Plojovic
Dzemail Smail Detanac
Suada Malicevic
Azra Kajevic
Dzenana Avdo Detanac
Mirza Corovic
author_facet Almir Kajevic
Haris Plojovic
Dzemail Smail Detanac
Suada Malicevic
Azra Kajevic
Dzenana Avdo Detanac
Mirza Corovic
author_sort Almir Kajevic
collection DOAJ
description FATCO syndrome (Fibular aplasia, tibial campomelia, and oligosyndactyly ) is a very rare malformation of an unknown genetic basis. It more commonly occurs in male children, and the lower extremities are more frequently affected. This is a case of a male newborn with the rare FATCO syndrome. It is the first child of healthy, unrelated parents. The pregnancy, being the first, was regular, monitored, and concluded with a cesarean section at 39 weekswithout any complications. The 33-year-old mother denies taking medication during pregnancy but reports having had COVID-19 in the fourth month of pregnancy. The newborn has normal upper extremities and the left lower extremity. The right lower extremity exhibits a shorter, curved lower leg with reduced circumference. A dimple is observed on the skin on the anterior side of the shin. There is a missing fifth toe on the right foot. Treatment involves a multidisciplinary approach and orthopedic-surgical corrections after birth to avoid varying degrees of disability.
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institution Kabale University
issn 1318-0347
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language English
publishDate 2024-12-01
publisher Slovenian Medical Association
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series Zdravniški Vestnik
spelling doaj-art-c944a5881aa64016aa39bf8fbf7ce6762025-01-04T17:56:06ZengSlovenian Medical AssociationZdravniški Vestnik1318-03471581-02242024-12-019311-1241041410.6016/ZdravVestn.35313090FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case reportAlmir Kajevic0Haris Plojovic1Dzemail Smail Detanac2Suada Malicevic3Azra Kajevic4Dzenana Avdo Detanac5Mirza Corovic6Department of Neonatology, General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of Surgery, the General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of Surgery, the General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of Neonatology, General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of General Medicine, General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of Ophtalmology, General hospital Novi Pazar, Novi Pazar, SerbiaDepartment of Surgery, the General hospital Novi Pazar, Novi Pazar, SerbiaFATCO syndrome (Fibular aplasia, tibial campomelia, and oligosyndactyly ) is a very rare malformation of an unknown genetic basis. It more commonly occurs in male children, and the lower extremities are more frequently affected. This is a case of a male newborn with the rare FATCO syndrome. It is the first child of healthy, unrelated parents. The pregnancy, being the first, was regular, monitored, and concluded with a cesarean section at 39 weekswithout any complications. The 33-year-old mother denies taking medication during pregnancy but reports having had COVID-19 in the fourth month of pregnancy. The newborn has normal upper extremities and the left lower extremity. The right lower extremity exhibits a shorter, curved lower leg with reduced circumference. A dimple is observed on the skin on the anterior side of the shin. There is a missing fifth toe on the right foot. Treatment involves a multidisciplinary approach and orthopedic-surgical corrections after birth to avoid varying degrees of disability.https://vestnik.szd.si/index.php/ZdravVest/article/view/3531fatco syfibular aplasiaoligosyndactylytibial campomelia
spellingShingle Almir Kajevic
Haris Plojovic
Dzemail Smail Detanac
Suada Malicevic
Azra Kajevic
Dzenana Avdo Detanac
Mirza Corovic
FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
Zdravniški Vestnik
fatco sy
fibular aplasia
oligosyndactyly
tibial campomelia
title FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
title_full FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
title_fullStr FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
title_full_unstemmed FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
title_short FATCO syndrome (fibular aplasia, tibial campomelia, and oligosyndactyly ) in newborn in Serbia – A case report
title_sort fatco syndrome fibular aplasia tibial campomelia and oligosyndactyly in newborn in serbia a case report
topic fatco sy
fibular aplasia
oligosyndactyly
tibial campomelia
url https://vestnik.szd.si/index.php/ZdravVest/article/view/3531
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