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B\u00fcy\u00fckgebiz B, Ozt\u00fcrk Y, Arslan N, Ozer E. A rare cause of protein-losing enteropathy and growth retardation in infancy: Infantile systemic hyalinosis. Turk J Pediatr. 2003; 45:258-260."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Hanks S, Adams S, Douglas J, et al. Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet. 2003; 73:791-800.","DOI":"10.1086\/378418"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Rahman N, Dunstan M, Teare MD, et al. The gene for juvenile hyaline fibromatosis maps to chromosome 4q21. Am J Hum Genet. 2002; 71:975-980.","DOI":"10.1086\/342776"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Huang YC, Xiao YY, Zheng YH, Jang W, Yang YL, Zhu XJ. Infantile systemic hyalinosis: A case report and mutation analysis in a Chinese infant. 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El-Kamah GhY, El-Darouti MA, Kotoury AIS, Mostafa IM.Farber disease syndrome verses stiff skin: Expanding the spectrum. Egyptian Journal of Medical Human Genetics. 2009; 10:135-142."},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Gupta LK, Singhi MK, Bansal M, Khullar R, Jain V, Kachhawa D. Juvenile hyaline fibromatosis in siblings. Indian J Dermatol Venerol Leprol. 2005; 71(2):115-118.","DOI":"10.4103\/0378-6323.13998"},{"key":"17","unstructured":"17. Hyaline Fibromatosis Syndrome. Includes: Infantile Systemic Hyalinosis, Juvenile Hyaline Fibromatosis: http:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1525\/, February 27, 2008; Last Update: April 11, 2013."},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Zand DJ, Huff D, Everman D, Russell K, Saitta S, McDonald-McGinn D, Zackai EH. Autosomal dominant inheritance of infantile myofibromatosis. Am J Med Genet A. 2004; 126A:261-266.","DOI":"10.1002\/ajmg.a.20598"},{"key":"19","unstructured":"19. Arbour L, Reilly C, McGillivray B, Prendiville J, Dimmick J. Infantile systemic hyalinosis: A rare syndrome of progressive, painful contractures with peculiar hyperpigmentation and death in infancy. 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