Progressive Pseudorheumatoid Dysplasia
What's New
Last Posted: Mar 15, 2023
- Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype-phenotype analysis of 105 patients.
Wang Wei, et al. World journal of pediatrics : WJP 2023 0 - Progressive pseudorheumatoid dysplasia: a rare childhood disease.
Torreggiani Sofia et al. Rheumatology international 2019 Mar 39(3) 441-452 - Association analysis on polymorphisms in WISP3 gene and developmental dysplasia of the hip in Han Chinese population: A case-control study.
Zhang Junxin, et al. Gene 2018 4 - WISP3 mutational analysis in Indian patients diagnosed with progressive pseudorheumatoid dysplasia and report of a novel mutation at p.Y198.
Madhuri V, et al. Bone & joint research 2016 7 (7) 301-6 - Progressive pseudorheumatoid dysplasia
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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