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: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Slovenian Medical Association
2024-12-01
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| Series: | Zdravniški Vestnik |
| Subjects: | |
| Online Access: | https://vestnik.szd.si/index.php/ZdravVest/article/view/3531 |
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| Summary: | 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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| ISSN: | 1318-0347 1581-0224 |