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Features include: Calcinosis, Scleroderma, Abnormality of chromosome stability, and Sclerodactyly and 3 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Skin | 1 | Telangiectasia |
Biomarker and diagnostic research for scleroderma, familial progressive has been reported in the published literature.
1 clinical trial registered, 1 recruiting. Interventions under study include drug therapy. Pipeline includes 1 PHASE2. Research is primarily industry-sponsored.
143 publications have been identified in PubMed for scleroderma, familial progressive. Research spans Review / Meta-Analysis (30%), Epidemiology / Natural History (28%), and Case Report / Case Series (19%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 38 | 30% |
Data assembled from 5 of 12 sources · Last updated Nov 3, 2026, 1:28 PM UTC
Online Mendelian Inheritance in Man
Disease patterns and progression |
36 |
28% |
Patient case studies | 24 | 19% |
Laboratory research | 24 | 19% |
Testing and diagnosis research | 2 | 2% |
Other research | 1 | 1% |
Clinical study results | 1 | 1% |
New treatment approaches | 1 | 1% |
Frazier W MD, MPH (2026). [PMID: 42101599](https://pubmed.ncbi.nlm.nih.gov/42101599/). *Am Fam Physician*. [Review / Meta-Analysis]
Padilla CM (2026). [PMID: 40771159](https://pubmed.ncbi.nlm.nih.gov/40771159/). *Arthritis Care Res (Hoboken)*. [Diagnostic / Biomarker]
Rodriguez-Martin I (2026). [PMID: 41999721](https://pubmed.ncbi.nlm.nih.gov/41999721/). *Lancet Rheumatol*. [Epidemiology / Natural History]
Pan J (2026). [PMID: 42136825](https://pubmed.ncbi.nlm.nih.gov/42136825/). *Open Life Sci*. [Review / Meta-Analysis]
Xiao Y (2026). [PMID: 41866288](https://pubmed.ncbi.nlm.nih.gov/41866288/). *Ann Rheum Dis*. [Basic Science / Preclinical]
Giovengo M (2026). [PMID: 41892626](https://pubmed.ncbi.nlm.nih.gov/41892626/). *Brain Sci*. [Review / Meta-Analysis]
Martínez-López J (2026). [PMID: 41236837](https://pubmed.ncbi.nlm.nih.gov/41236837/). *Arthritis Rheumatol*. [Epidemiology / Natural History]
Aiton E (2026). [PMID: 41851855](https://pubmed.ncbi.nlm.nih.gov/41851855/). *BMC Med*. [Epidemiology / Natural History]
Fontes-Dantas FL (2026). [PMID: 41219597](https://pubmed.ncbi.nlm.nih.gov/41219597/). *Adv Exp Med Biol*. [Review / Meta-Analysis]
Adigun R (2026). [PMID: 28613625](https://pubmed.ncbi.nlm.nih.gov/28613625/). *Unknown Journal*. [Review / Meta-Analysis]
AI-curated news mentioning scleroderma, familial progressive
Updated Oct 19, 2026
A recent study published in PubMed highlights health literacy levels among individuals with systemic sclerosis, utilizing data from the Scleroderma Patient-Centered Intervention Network (SPIN). This cross-sectional study aims to inform future interventions to improve patient outcomes.
CAR-T cell therapy, traditionally used for blood cancers, is being explored for autoimmune diseases such as lupus, multiple sclerosis, and scleroderma. Experts believe this innovative approach could revolutionize treatment for these challenging conditions.
Yale School of Medicine is advancing CAR-T therapy beyond oncology, initiating clinical trials for autoimmune diseases such as lupus, multiple sclerosis, and scleroderma. This innovative approach could reshape treatment paradigms for these conditions.
A recent study highlights the complexities of managing scleroderma renal crisis and associated cardiac complications in a young patient with mixed connective tissue disease (MCTD). The case emphasizes the need for further research into the implications of anti-U3 RNP and anti-RNA polymerase III antibodies.
Recent research highlights the occurrence of scleroderma renal crisis in patients with mixed connective tissue disease, providing new insights into this rare complication. Understanding this association may improve clinical management and patient outcomes.