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Feingold Syndrome

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Atlas of Genetic Diagnosis and Counseling

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Abstract

Feingold in 1975 originally described a father, son, and grandmother with microcephaly, hand abnormalities, tracheoesophageal fistula, duodenal atresia, and normal intelligence. Later in 1978, Feingold reported a mother and daughter with similar findings except for the absence of tracheoesophageal fistula and duodenal atresia.

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References

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Authors and Affiliations

  1. Medical Genetics, Shriners Hospitals for Children, Perinatal and Clinical Genetics, Department of Pediatrics, LSU Health Sciences Center, Shreveport, LA, USA

    Harold Chen

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  1. Harold Chen
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Chen, H. (2017). Feingold Syndrome. In: Atlas of Genetic Diagnosis and Counseling. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2401-1_258

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  • DOI: https://doi.org/10.1007/978-1-4939-2401-1_258

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  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4939-2400-4

  • Online ISBN: 978-1-4939-2401-1

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