CONORENAL SYNDROME: REPORT OF A CASE

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SHARIFIAN M.; GHOUJEHVAND N.

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Journal: Research in Medicine Year:2005 | Volume:29 | Issue:1 Page(s): 67-70

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Information Journal Paper

Title

CONORENAL SYNDROME: REPORT OF A CASE

Author(s)

SHARIFIAN M. | GHOUJEHVAND N. | Issue Writer Certificate

Keywords

CONORENAL SYNDROMEQ4

SALDINO MAINZERQ3

MULTIPLE EPIPHYSEAL DYSPLASIAQ4

RETINITIS PIGMENTOSAQ4

CHILDRENQ4

Abstract

CONORENAL SYNDROME or SALDINO MAINZER is a rare hereditary disease characterized by cone-shaped epiphyses of the phalanges, RETINITIS PIGMENTOSA and renal manifestations (nephropathy). Case report: Herein we report an eight years old girl with a collection of signs and symptoms compatible with CONORENAL SYNDROME. She first presented with ductility's, dysuria, frequency, discolored urine and progressive generalized edema. Renal biopsy revealed tubular atrophy, interstitial fibrosis and thickening of the glomerular basement membrane. This constellation of signs and symptoms is compatible with CONORENAL SYNDROME.

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APA: Copy

SHARIFIAN, M., & GHOUJEHVAND, N.. (2005). CONORENAL SYNDROME: REPORT OF A CASE. PAJOUHESH DAR PEZESHKI, 29(1), 67-70. SID. https://sid.ir/paper/41842/en

Vancouver: Copy

SHARIFIAN M., GHOUJEHVAND N.. CONORENAL SYNDROME: REPORT OF A CASE. PAJOUHESH DAR PEZESHKI[Internet]. 2005;29(1):67-70. Available from: https://sid.ir/paper/41842/en

IEEE: Copy

M. SHARIFIAN, and N. GHOUJEHVAND, “CONORENAL SYNDROME: REPORT OF A CASE,” PAJOUHESH DAR PEZESHKI, vol. 29, no. 1, pp. 67–70, 2005, [Online]. Available: https://sid.ir/paper/41842/en

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