Researchers Report Rare Case of Kartagener Syndrome with Minimal Change Disease in a 24-year-old Woman
China: In an unusual clinical presentation, Hua Zhou, Department of Nephrology, Shengjing Hospital of China Medical University, Liaoning, China, and colleagues have reported a rare case of a young woman diagnosed with Kartagener syndrome who also developed minimal change disease, a form of nephrotic syndrome. According to them, the case is considered the first documented instance of such a combination, highlighting the need for awareness and tailored treatment approaches when multisystem disorders co-exist.
The case, published in the Journal of Medical Case Reports, concerns a 24-year-old woman from China who sought medical attention with complaints of foamy urine lasting two weeks and swelling around her eyelids and legs for one week. On evaluation, she was diagnosed with nephrotic syndrome, and further investigations pointed to a much rarer underlying condition.
Imaging studies revealed features consistent with Kartagener syndrome — a genetic disorder characterized by a classic triad of bronchiectasis, chronic sinusitis, and complete reversal of internal organ positioning (situs inversus). The patient had a known history of recurrent respiratory tract infections and dextrocardia from childhood, which aligned with the diagnosis. A renal biopsy later confirmed the presence of minimal change disease, explaining the proteinuria and low serum albumin levels.
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