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Article

Adams-Oliver Syndrome: A Comprehensive Literature Review of Clinical, Nutritional, Genetic, and Molecular Aspects with Nursing Care Considerations.

International journal of molecular sciences - 23 Dec 2025

Badiu Tișa Ioana, Cozma-Petruț Anamaria, Chiorean Alin-Dan, Miere Doina, Filip Lorena, Banc Roxana, Mîrza Oana, Bordea Mădălina Adriana

Abstract excerpt

The present review aims to provide a comprehensive overview of the current literature on Adams-Oliver syndrome (AOS), synthesizing information on its clinical features, genetic and molecular underpinnings, nutritional aspects, and key nursing care considerations. AOS is a rare congenital disorder. Its genetic basis is heterogeneous, involving mutations in at least six key genes (ARHGAP31, RBPJ, NOTCH1, DLL4,...

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Share to Ectodermal Dysplasia
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Limb Deformities, Congenital

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Source

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Identifiers

PMID: 41516051
DOI: 10.3390/ijms27010173
PMCID: PMC12786322

Genes

ARHGAP31
DLL4
DOCK6
EOGT
NOTCH1
RBPJ

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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