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Supplementary data from the Bartter syndrome systematic review characterize the clinical spectrum of this rare renal tubular disorder. The heterogeneous presentation across case reports underscores the importance of genetic testing for accurate subtype classification.
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![Figure 9: Supplementary data from the Bartter syndrome systematic review characterize the clinical spectrum of this rare renal tubular disorder. The heterogeneous presentation across case reports underscores the importance of genetic testing for accurate subtype classification.]() > Source: Rakhtan K Qasba et al. "Bartter Syndrome: A Systematic Review of Case Reports and Case Series.." *Medicina (Kaunas, Lithuania)*, 2023. PMID: [37763757](https://pubmed.ncbi.nlm.nih.gov/37763757/)
<figure> <img src="" alt="Supplementary data from the Bartter syndrome systematic review characterize the clinical spectrum of this rare renal tubular disorder. The heterogeneous presentation across case reports underscores the importance of genetic testing for accurate subtype classification." /> <figcaption>Figure 9. Supplementary data from the Bartter syndrome systematic review characterize the clinical spectrum of this rare renal tubular disorder. The heterogeneous presentation across case reports underscores the importance of genetic testing for accurate subtype classification.<br> Source: Rakhtan K Qasba et al. "Bartter Syndrome: A Systematic Review of Case Reports and Case Series.." <em>Medicina (Kaunas, Lithuania)</em>, 2023. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/37763757/">37763757</a></figcaption> </figure>