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ABSTRACT: Introduction
Fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome is a rare disorder with unknown molecular basis. Since it is a rare disorder, so it is commendable to report the each case, due to its sporadic incidence and paucity of the standardized management protocol for their management.Case report
It is a case report of newly born male baby, whose anxious parents presented to the outpatient department with a deformity in the left lower limb. This resembled the FATCO syndrome. After clinico-radiological workup, it was categorized as a variant of FATCO syndrome.Conclusion
Counseling of parents should be done and let them realize that what is inescapable with this syndrome and what is bound to happen during the treatment.
SUBMITTER: Mishra PK
PROVIDER: S-EPMC8686498 | biostudies-literature |
REPOSITORIES: biostudies-literature