Renal involvement in Fabry disease from Tunisian families: Six case reports

doi:10.5527/wjn.v15.i2.109420

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World Journal of Nephrology

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2220-6124

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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.

World J Nephrol. Jun 25, 2026; 15(2): 109420
Published online Jun 25, 2026. doi: 10.5527/wjn.v15.i2.109420

Table 1 Baseline characteristics of Fabry disease patients

Patient ID	Age	Sex	Hypertension	Proteinuria (g/24 hours)	eGFR (mL/minute)	Extra-renal manifestations
A.1	29	Male	Yes	5.5	23.7	Angiokeratoma, LVH, acroparesthesia, deafness
B.1	20	Male	Yes	2.6	75.1	Angiokeratoma, seizure, LVH
B.2	22	Male	No	2.8	77.4	None
C.1	25	Male	No	1.3	127	Angiokeratoma, anhidrosis, acroparesthesia
C.2	23	Male	No	Negative	130	None
C.3	16	Female	No	Negative	135	None

eGFR: Estimated glomerular filtration rate; LVH: Left ventricular hypertrophy.

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Citation: Tlili S, Ghabi H, Mami I, Ben Hmida F, Rais L, Zouaghi MK. Renal involvement in Fabry disease from Tunisian families: Six case reports. World J Nephrol 2026; 15(2): 109420
URL: https://www.wjgnet.com/2220-6124/full/v15/i2/109420.htm
DOI: https://dx.doi.org/10.5527/wjn.v15.i2.109420

Tlili S, Ghabi H, Mami I, Ben Hmida F, Rais L, Zouaghi MK. Renal involvement in Fabry disease from Tunisian families: Six case reports. World J Nephrol 2026; 15(2): 109420 [PMID: 42395686 DOI: 10.5527/wjn.v15.i2.109420]

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