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- W4210641808 abstract "The syndrome of fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO syndrome) is a rare genetic disease that has been increasingly reported over the past 40 years. We report the case of a newborn boy with unilateral skeletal abnormalities that were evident clinically and radiologically. The baby was an infant of a diabetic mother, and the Egyptian parents were consanguineous with a strong family history of genetic diseases and congenital anomalies. Besides describing a new case report of this syndrome, we emphasize the importance of prenatal diagnosis and genetic counseling, especially for families at high risk for genetic diseases in developing countries." @default.
- W4210641808 created "2022-02-08" @default.
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- W4210641808 date "2022-01-28" @default.
- W4210641808 modified "2023-10-18" @default.
- W4210641808 title "Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight" @default.
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- W4210641808 doi "https://doi.org/10.7759/cureus.21702" @default.
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