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Article

A Feingold syndrome case with previously undescribed features and a new mutation.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2009

Koçak H, Ozaydin E, Köse G, Marcelis C L M, Kamsteeg E J, Ceylaner S

Abstract excerpt

Feingold syndrome (FS) is a dominantly inherited combination of microcephaly with or without learning disabilities, hand and foot abnormalities, short palpebral fissures and esophageal/duodenal atresia. The syndrome has autosomal dominant inheritance with full penetrance, and variable expressivit...

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Source

Identifiers

PMID: 19852433

Genes

MYCN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19852433-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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