1. Spencer CH, Patwardhan A. Pediatric rheumatology for the primary care clinicians-recognizing patterns of disease. Current problems in pediatric and adolescent health care. 2015;45(7):185–206.
2. Calder AD, Foley P. Skeletal dysplasias: an overview. Paediatrics and Child Health. 2018;28(2):84–92.
3. Madhusudan S, Gupta A, Prakash M, Matta D, Suri D, Singh S. Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome: a mimicker of juvenile idiopathic arthritis. Scand J Rheumatol. 2016;45:77 − 8.
4. Garcia Segarra N, Mittaz L, Campos-Xavier AB, Bartels CF, Tuysuz B, Alanay Y, et al., editors. The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals. American Journal of Medical Genetics Part C: Seminars in Medical Genetics; 2012: Wiley Online Library.
5. Albuhairan I, Al-Mayouf SM, editors. Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: Clinical and molecular genetic findings in 22 patients. Seminars in arthritis and rheumatism; 2013: Elsevier.
6. Al-Mayouf SM. Noninflammatory disorders mimic juvenile idiopathic arthritis. International Journal of Pediatrics and Adolescent Medicine. 2018;5(1):1–4.
7. Offiah AC, Woo P, Prieur A-M, Hasson N, Hall CM. Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy. American Journal of Roentgenology. 2005;185(2):522-9.
8. Neyzi O, Bundak R, Gökçay G, Günöz H, Furman A, Darendeliler F, et al. Reference values for weight, height, head circumference, and body mass index in Turkish children. Journal of clinical research in pediatric endocrinology. 2015;7(4):280.
9. Kurt-Sukur ED, Simsek‐Kiper PO, Utine GE, Boduroglu K, Alanay Y. Experience of a skeletal dysplasia registry in Turkey: A five‐years retrospective analysis. American Journal of Medical Genetics Part A. 2015;167(9):2065-74.
10. Bowyer S, Roettcher P. Pediatric rheumatology clinic populations in the United States: results of a 3 year survey. Pediatric Rheumatology Database Research Group. The Journal of Rheumatology. 1996;23(11):1968-74.
11. Rosenberg AM. Longitudinal analysis of a pediatric rheumatology clinic population. The Journal of rheumatology. 2005;32(10):1992–2001.
12. Unger S. A genetic approach to the diagnosis of skeletal dysplasia. Clinical Orthopaedics and Related Research (1976–2007). 2002;401:32 − 8.
13. Brown R, Monsell F. Understanding the skeletal dysplasias. Current Orthopaedics. 2003;17(1):44–55.
14. Solomon BD, Muenke M. When to suspect a genetic syndrome. American family physician. 2012;86(9):826.
15. Matuszewska G, Zaniewicz-Kaniewska K, Włodkowska-Korytkowska M, Smorawińska P, Saied F, Kunisz W, et al. Radiological imaging in pediatric rheumatic diseases. Polish journal of radiology. 2014;79:51.
16. Colebatch-Bourn A, Edwards C, Collado P, D'Agostino M, Hemke R, Jousse-Joulin S, et al. EULAR-PReS points to consider for the use of imaging in the diagnosis and management of juvenile idiopathic arthritis in clinical practice. Annals of the Rheumatic Diseases. 2015;74(11):1946-57.
17. Taşar M, Eyileten Z, Kasımzade F, Uçar T, Kendirli T, Uysalel A. Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. J Pediatr. 2014;56:684-6.
18. Jay G, Torres J, Warman M, Laderer M, Breuer K. The role of lubricin in the mechanical behavior of synovial fluid. Proceedings of the National Academy of Sciences. 2007;104(15):6194-9.
19. Mannurita SC, Vignoli M, Bianchi L, Kondi A, Gerloni V, Breda L, et al. CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort. European Journal of Human Genetics. 2014;22(2):197–201.
20. Pode-Shakked B, Vivante A, Barel O, Padeh S, Marek-Yagel D, Veber A, et al. Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature. BMC medical genetics. 2019;20(1):53.
21. Giray E, Yağcı İ, Elçioğlu HN. Progressive pseudorheumotoid dysplasia: A presentation of four cases with slow and rapid progression and effects of early rehabilitation program. Turkish journal of physical medicine and rehabilitation. 2019;65(3):290.
22. Adak B, Tekeoĝlu I, Sakarya M, Uĝra S. Progressive pseudorheumatoid chondrodysplasia: a hereditary disorder simulating rheumatoid arthritis. Clinical rheumatology. 1998;17(4):343-5.
23. Vaccaro M, Guarneri C, Blandino A. Trichorhinophalangeal syndrome. Journal of the American Academy of Dermatology. 2005;53(5):858 − 60.
24. Maas S, Shaw A, Bikker H, Hennekam RC. Trichorhinophalangeal syndrome. 2017.
25. Girschick H, Wolf C, Morbach H, Hertzberg C, Lee-Kirsch MA. Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene. Pediatric Rheumatology. 2015;13(1):37.
26. Bilginer Y, Düzova A, Topaloğlu R, Batu E, Boduroğlu K, Güçer Ş, et al. Three cases of spondyloenchondrodysplasia (SPENCD) with systemic lupus erythematosus: a case series and review of the literature. Lupus. 2016;25(7):760-5.
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