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Article

MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.

American journal of medical genetics - 22 Aug 1997

Frydman M, Katz M, Cabot S G, Soen G, Kauschansky A, Sirota L

Abstract excerpt

We report on 4 families with microcephaly, type A brachydactyly, variable learning disabilities, short stature, duodenal atresia, patent ductus arteriosus (PDA), hallux valgus, restricted elbow and finger movements, and amesophalangy and syndactyly of toes. Three previous families manifested all signs of the syndrome, and in another four reports the phenotype was incomplete. These cases are reviewed. Penetrance...

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Source

Identifiers

PMID: 9268091
DOI: 10.1002/(sici)1096-8628(19970822)71:3<251::aid-ajmg1>3.0.co;2-x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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