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

[Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Feb 2014

Huang Shan, Liang Yan, Wu Wei, Fu Xi, Liao Lihong, Luo Xiaoping

Abstract excerpt

OBJECTIVE: To explore clinical, radiographical and genetic characteristics of classical Hutchinson-Gilford progeria syndrome (HGPS). METHOD: Data of a case of HGPS diagnosed at Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology was analyzed and related literature was reviewed. RESULT: At the age of 8 months, the affected-infant presented with characteristic...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Lamin Type A

Share to Lower Extremity

Share to Progeria

Share to Skin Diseases

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 24739722

Genes

LMNA

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].PMID 24739722Read ↗

Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.Semantic proximity Read ↗

Epidemiological characteristics of patients with Hutchinson-Gilford progeria syndrome and progeroid laminopathies in China.Semantic proximity Read ↗

Hutchinson-Gilford progeria syndrome: review of the phenotype.Semantic proximity Read ↗

[Three cases of Hutchinson-Gilford progeria syndrome].Semantic proximity Read ↗

The clinical characteristics of Asian patients with classical-type Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Hutchinson-Gilford Progeria syndrome: Report of the first Togolese case.Semantic proximity Read ↗

Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation.Semantic proximity Read ↗

Skin signs as early manifestations of Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Mini-Review: molecular elucidations of hutchinson-gilford progeria syndrome: A hope for managing horrors of premature aging in children.Semantic proximity Read ↗

Hutchinson-Gilford progeria syndrome: report of 2 cases and a novel LMNA mutation of HGPS in China.Semantic proximity Read ↗

Phenotype and course of Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Why and How Are Infants with Hutchinson-Gilford Progeria Syndrome Born Without Severe Manifestations?Semantic proximity Read ↗

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