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lüll A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis Buyukgebiz B; Ozturk Y; Arslan N; Ozer ETurk J Pediatr 2003[Jul]; 45 (3): 258-60Infantile systemic hyalinosis is a rare, progressive, fatal condition with a presumably autosomal recessive mode of inheritance. It is characterized by widespread deposition of hyaline material in many tissues. We present a three-month-old girl with hypoproteinemia, growth retardation, and generalized stiff and edematous skin, who was diagnosed as protein-losing enteropathy. A final diagnosis of systemic hyalinosis was made. In this report, we present a very rare entity of infantile systemic hyalinosis, which is a cause of protein-losing enteropathy and growth retardation in infancy, and review the relevant literature.|Connective Tissue Diseases/*complications/diagnosis[MESH]|Developmental Disabilities/diagnosis[MESH]|Diagnosis, Differential[MESH]|Female[MESH]|Humans[MESH]|Hyalin/*metabolism[MESH]|Infant[MESH]|Protein-Losing Enteropathies/*complications/diagnosis[MESH]|Skin Diseases/*complications/diagnosis[MESH] |