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Article

Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.

Archives of dermatology - 1 May 2009

González-Enseñat M Antonia, Vicente Asunción, Poo Pilar, Catalá Vicenç, Mar Pérez-Iribarne M, Fuster Carme, Geán Esther, Happle Rudolf

Abstract excerpt

BACKGROUND: Phylloid hypomelanosis is a rare neurocutaneous syndrome characterized by a pattern of hypopigmentation consisting of leaflike or oblong macules reminiscent of floral ornaments. Associated extracutaneous anomalies include cerebral, ocular, and skeletal defects. Recently it has been suggested that this phenotype originates from mosaic partial or complete trisomy 13. We report clinical and cytogenetic...

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Identifiers

PMID: 19451503
DOI: 10.1001/archdermatol.2009.37

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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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