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

[Histopathological and genetical diagnosis of one case of neonatal ectodermal dysplasia/skin fragility syndrome].

Zhonghua shao shang za zhi = Zhonghua shaoshang zazhi = Chinese journal of burns - 20 Jun 2020

Ruan Q F, Xia C, Xie W G

Abstract excerpt

On August 6, 2015, a male infant with ectodermal dysplasia/skin fragility syndrome at 6 hours of birth was admitted to the Burn Department of Tongren Hospital of Wuhan University & Wuhan Third Hospital. The ulcerous skin tissue in thoracic area was harvested. The histopathological change of wound tissue was observed with hematoxylin-eosin staining. The result showed that the epidermal muscle cell layer was...

Read the complete abstract on PubMed

Topics

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

Share to Ectodermal Dysplasia
Share to Epidermis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Mutation

Share to Plakophilins

Share to Skin Diseases

Source

Identifiers

PMID: 32594712
DOI: 10.3760/cma.j.cn501120-20190329-00148

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Histopathological and genetical diagnosis of one case of neonatal ectodermal dysplasia/skin fragility syndrome].PMID 32594712Read ↗

[Genetic diseases with skin fragility in children].Semantic proximity Read ↗

Ectodermal dysplasia-skin fragility syndrome with a new mutation.Semantic proximity Read ↗

[Neonatal hereditary dystrophic epidermolysis bullosa: a genetically diagnosed case report].Semantic proximity Read ↗

Molecular and diagnostic aspects of genetic skin fragilitySemantic proximity Read ↗

Ectodermal dysplasia-skin fragility syndrome: two new cases with a novel missense mutation.Semantic proximity Read ↗

A 2-year-old girl with skin fragility.Semantic proximity Read ↗

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1.Semantic proximity Read ↗

[Developmental genes: definitions and contribution to skin biology].Semantic proximity Read ↗

Ectodermal dysplasia-skin fragility syndrome resulting from a new homozygous mutation, 888delC, in the desmosomal protein plakophilin 1.Semantic proximity Read ↗

[Focal dermal hypoplasia associated with pathogenic PORCN gene variant in postzygotic, unilateral mosaic form].Semantic proximity Read ↗

A case of mosaicism in ectodermal dysplasia-skin fragility syndrome.Semantic proximity Read ↗

A newborn with widespread skin lesions and extremity anomalies.Semantic proximity Read ↗

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