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Article

Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features.

Acta paediatrica (Oslo, Norway : 1992) - 1 Dec 2008

Mussa Alessandro, Baldassarre Giuseppina, Rosaia De Santis Lucia, Gastaldi Roberto, Corrias Andrea, Silengo Margherita Cirillo

Abstract excerpt

AIM: PHACES syndrome is a neurocutaneous condition characterized by the coexistence of large facial haemangiomas and at least one feature among posterior fossa malformations, cardiac and arterial anomalies, eye defects and sternal clefting. We review and discuss the phenotypes and the endocrine a...

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Identifiers

PMID: 18801022
DOI: 10.1111/j.1651-2227.2008.01032.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18801022-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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