CONGENITAL GENERALIZED LIPODYSTROPHY, COINCIDENT WITH PORTAL HYPERTENSION: A CASE REPORT AND REVIEW OF LITERATURE

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PARTOVI S.; SHARIFI D.; KHALESI H.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Journal: GOVARESH Journal Year:2004 | Volume:9 | Issue:4 Page(s): 248-250

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Information Journal Paper

Title

CONGENITAL GENERALIZED LIPODYSTROPHY, COINCIDENT WITH PORTAL HYPERTENSION: A CASE REPORT AND REVIEW OF LITERATURE

Author(s)

PARTOVI S. | SHARIFI D. | KHALESI H. | Issue Writer Certificate

Keywords

CONGENITAL GENERALIZED LIPODYSTROPHYQ4

CIRRHOSISQ2

PORTAL HYPERTENSIONQ4

Abstract

CONGENITAL GENERALIZED LIPODYSTROPHY (CGL) is a rare and progressive disorder (1 in 12 milion). Common clinical manifestations are lipoatrophy, acromegaloid feature, acanthosis nigricans, Hyperlipidemia, diabetes mellitus or abnormal glucose tolerance test. Rarely fatty liver and CIRRHOSIS is seen. The highest number reported in literature is 8 cases from Brazil and 6 cases from Scandinavia, respectively. The oldest case was a 19-year-old girl. Our case is a 13-year-old male with all above manifestations, also he had liver CIRRHOSIS. Another case of CGL had been reported by first author of this article, 13 years ago in Iranian Medical Journal.

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APA: Copy

PARTOVI, S., SHARIFI, D., & KHALESI, H.. (2004). CONGENITAL GENERALIZED LIPODYSTROPHY, COINCIDENT WITH PORTAL HYPERTENSION: A CASE REPORT AND REVIEW OF LITERATURE. GOVARESH JOURNAL, 9(4), 248-250. SID. https://sid.ir/paper/86247/en

Vancouver: Copy

PARTOVI S., SHARIFI D., KHALESI H.. CONGENITAL GENERALIZED LIPODYSTROPHY, COINCIDENT WITH PORTAL HYPERTENSION: A CASE REPORT AND REVIEW OF LITERATURE. GOVARESH JOURNAL[Internet]. 2004;9(4):248-250. Available from: https://sid.ir/paper/86247/en

IEEE: Copy

S. PARTOVI, D. SHARIFI, and H. KHALESI, “CONGENITAL GENERALIZED LIPODYSTROPHY, COINCIDENT WITH PORTAL HYPERTENSION: A CASE REPORT AND REVIEW OF LITERATURE,” GOVARESH JOURNAL, vol. 9, no. 4, pp. 248–250, 2004, [Online]. Available: https://sid.ir/paper/86247/en

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