{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,7]],"date-time":"2024-08-07T22:35:28Z","timestamp":1723070128960},"reference-count":13,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,9,10]]},"DOI":"10.7759\/cureus.17875","type":"journal-article","created":{"date-parts":[[2021,9,10]],"date-time":"2021-09-10T13:29:04Z","timestamp":1631280544000},"source":"Crossref","is-referenced-by-count":1,"title":["Osteoarticular Manifestations of Prolidase Deficiency and Disability: Case Reports of Two Moroccan Sisters"],"prefix":"10.7759","author":[{"given":"Mouna","family":"Asly","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Madiha","family":"Eljazouly","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.3390\/biology9050108","article-title":"Clinical genetics of prolidase deficiency: an updated review","volume":"9","author":"Spodenkiewicz M","year":"2020","unstructured":"Spodenkiewicz M, Spodenkiewicz M, Cleary M, et al.. Clinical genetics of prolidase deficiency: an updated review. Biology (Basel). 2020, 9:10.3390\/biology9050108","journal-title":"Biology (Basel)"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.b.30945","article-title":"A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability","volume":"153B","author":"Falik-Zaccai TC","year":"2010","unstructured":"Falik-Zaccai TC, Khayat M, Luder A, et al.. A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability. Am J Med Genet B Neuropsychiatr Genet. 2010, 153B:46-56. 10.1002\/ajmg.b.30945","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1979.04010010034010","article-title":"Prolidase deficiency: its dermatological manifestations and some additional biochemical studies","volume":"115","author":"Arata J","year":"1979","unstructured":"Arata J, Umemura S, Yamamoto Y, Hagiyama M, Nohara N. Prolidase deficiency: its dermatological manifestations and some additional biochemical studies. Arch Dermatol. 1979, 115:62-67. 10.1001\/archderm.1979.04010010034010","journal-title":"Arch Dermatol"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1981.01650110011009","article-title":"Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcers","volume":"117","author":"Ogata A","year":"1981","unstructured":"Ogata A, Tanaka S, Tomoda T, Murayama E, Endo F, Kikuchi I. Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcers. Arch Dermatol. 1981, 117:689-697. 10.1001\/archderm.1981.01650110011009","journal-title":"Arch Dermatol"},{"key":"ref5","article-title":"Ultrastructural studies on dermis from prolidase deficient subjects","volume":"23","author":"Pasquali Ronchetti I","year":"1991","unstructured":"Pasquali Ronchetti I, Quaglino D Jr, Dyne KM, Zanaboni G, Cetta G. Ultrastructural studies on dermis from prolidase deficient subjects. J Submicrosc Cytol Pathol. 1991, 23:439-45.","journal-title":"J Submicrosc Cytol Pathol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1136\/adc.76.5.441","article-title":"Prolidase deficiency and systemic lupus erythematosus","volume":"76","author":"Shrinath M","year":"1997","unstructured":"Shrinath M, Walter JH, Haeney M, Couriel JM, Lewis MA, Herrick AL. Prolidase deficiency and systemic lupus erythematosus. Arch Dis Child. 1997, 76:441-4. 10.1136\/adc.76.5.441","journal-title":"Arch Dis Child"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1016\/j.bone.2014.11.009","article-title":"Lack of prolidase causes a bone phenotype both in human and in mouse","volume":"72","author":"Besio R","year":"2015","unstructured":"Besio R, Maruelli S, Gioia R, et al.. Lack of prolidase causes a bone phenotype both in human and in mouse. Bone. 2015, 72:53-64. 10.1016\/j.bone.2014.11.009","journal-title":"Bone"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.jbspin.2009.07.004","article-title":"Prolidase deficiency: a rare aetiology of arthritis","volume":"77","author":"Marotte H","year":"2010","unstructured":"Marotte H, Gineyts E, Miossec P. Prolidase deficiency: a rare aetiology of arthritis. Joint Bone Spine. 2010, 77:88-9. 10.1016\/j.jbspin.2009.07.004","journal-title":"Joint Bone Spine"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320190319","article-title":"Clinical and biochemical characteristics of prolidase deficiency in siblings","volume":"19","author":"Freij BJ","year":"1984","unstructured":"Freij BJ, Levy HL, Dudin G, Mutasim D, Deeb M, Der Kaloustian VM. Clinical and biochemical characteristics of prolidase deficiency in siblings. Am J Med Genet. 1984, 19:561-71. 10.1002\/ajmg.1320190319","journal-title":"Am J Med Genet"},{"key":"ref10","article-title":"Prolidase deficiency: dento-facial aspects in a paediatric patient","volume":"15","author":"Lacarbonara M","year":"2014","unstructured":"Lacarbonara M, Cazzolla AP, Lacarbonara VA, Di Venere D, Capogreco M, Marzo G. Prolidase deficiency: dento-facial aspects in a paediatric patient. Eur J Paediatr Dent. 2014, 15:224-8.","journal-title":"Eur J Paediatr Dent"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1016\/j.jpeds.2007.03.025","article-title":"Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association","volume":"150","author":"Luder AS","year":"2007","unstructured":"Luder AS, Mandel H, Khayat M, Gurevich I, Frankel P, Rivlin J, Falik-Zaccai TC. Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association. J Pediatr. 2007, 150:656-8. 10.1016\/j.jpeds.2007.03.025","journal-title":"J Pediatr"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2009.12.038","article-title":"An Amish boy with recurrent ulcerations of the lower extremities, telangiectases of the hands, and chronic lung disease","volume":"62","author":"Kelly JJ","year":"2010","unstructured":"Kelly JJ, Freeman AF, Wang H, Cowen EW, Kong HH. An Amish boy with recurrent ulcerations of the lower extremities, telangiectases of the hands, and chronic lung disease. J Am Acad Dermatol. 2010, 62:1031-4. 10.1016\/j.jaad.2009.12.038","journal-title":"J Am Acad Dermatol"},{"key":"ref13","article-title":"Prolidase deficiency","author":"Ferreira C","year":"2015","unstructured":"Ferreira C, Wang H. Prolidase deficiency. GeneReviews\u00ae [Internet]. Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, (ed): University of Washington, Seattle, Seattle (WA); 2015. https:\/\/pubmed.ncbi.nlm.nih.gov\/26110198\/"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/65673-osteoarticular-manifestations-of-prolidase-deficiency-and-disability-case-reports-of-two-moroccan-sisters","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:33:53Z","timestamp":1707507233000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/65673-osteoarticular-manifestations-of-prolidase-deficiency-and-disability-case-reports-of-two-moroccan-sisters"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,9,10]]},"references-count":13,"URL":"https:\/\/doi.org\/10.7759\/cureus.17875","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,9,10]]}}}