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Article

Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.

Acta dermato-venereologica - 1 Jan 2008

Castori Marco, Ruggieri Salvatore, Giannetti Luca, Annessi Giorgio, Zambruno Giovanna

Abstract excerpt

Schöpf-Schulz-Passarge syndrome is a rare ectodermal dysplasia, characterized chiefly by multiple eyelid apocrine hidrocystomas, palmo-plantar keratoderma, hypodontia, hypotrichosis and nail dystrophy. The clinical spectrum and the most likely inheritance pattern(s) have not yet been completely d...

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Source

Identifiers

PMID: 19002348
DOI: 10.2340/00015555-0547

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19002348-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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