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Article

Catel-Manzke syndrome without Manzke dysostosis.

American journal of medical genetics. Part A - 1 Mar 2020

Miller Danny E, Chow Penny, Gallagher Emily R, Perkins Jonathan A, Wenger Tara L

Abstract excerpt

Catel-Manzke syndrome is characterized by hand anomalies, Robin sequence, cardiac defects, joint hyperextensibility, and characteristic facial features. Approximately 40 patients with Catel-Manzke have been reported, all with the pathognomonic bilateral or unilateral hyperphalangy caused by an accessory bone between the second metacarpal and proximal phalanx known as Manzke dysostosis. Here we present the first...

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Identifiers

PMID: 31833187
DOI: 10.1002/ajmg.a.61436

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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