Article

A new variant of MYCN gene as a cause of Feingold syndrome

2022-03-03

Abstract excerpt

Feingold syndrome-1 (FS1) is a rare disorder that is inherited in autosomal dominant manner. The most common phenotypical features described are finger and toe anomalies, microcephaly, short stature and intestinal atresia. Here, we present a 7-year-old boy with severe intellectual disability who is diagnosed with FS1 syndrome.

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Literature Corpus work: 319fa8b2-2adc-55c0-b94d-0ae81854cb59
DOI: 10.22541/au.164634028.81182459/v1

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