Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias.

Pediatric dermatology - 1 Sept 2016

Whittington Adam, Stein Sarah, Kenner-Bell Brandi

Abstract excerpt

Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome is a rare form of autosomal dominant ectodermal dysplasia due to mutations in the TP63 gene, a locus that has also been implicated in other syndromic forms of ectodermal dysplasia. It shares many phenotypic characteristics with other TP63 gene mutation syndromes, often making an accurate diagnosis difficult. Long-term management and follow-up of the various...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anodontia
Share to Breast
Share to Ectodermal Dysplasia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Limb Deformities, Congenital

Share to Mothers

Share to Nails, Malformed

Share to Pigmentation Disorders

Share to Siblings

Source

Identifiers

PMID: 27469932
DOI: 10.1111/pde.12938

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias.PMID 27469932Read ↗

Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63.Semantic proximity Read ↗

ADULT syndrome due to an R243W mutation in TP63.Semantic proximity Read ↗

TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes.Semantic proximity Read ↗

EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report.Semantic proximity Read ↗

Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome.Semantic proximity Read ↗

Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expression.Semantic proximity Read ↗

Ectodermal Dysplasia – An Overview and UpdateSemantic proximity Read ↗

Further phenotypic and genetic variation in ADULT syndrome.Semantic proximity Read ↗

Mutation analysis of p63 gene in the first Chinese family with ADULT syndrome.Semantic proximity Read ↗

A spectrum of TP63-related disorders with eight affected individuals in five unrelated families.Semantic proximity Read ↗

Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.Semantic proximity Read ↗

Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.