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Middle Syndrome (Pseudoaldosteronsim) OMIT 177200 Gene: SCNN1B; SCNN1G Locus: 16p13-p12 OMIT: 600760; 600761 SERVICE: mutation analysis of exon 12 in both the SCNN1B and SCNN1G genes TESTING: Diagnostic*:
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What is liddle syndrome pseudoaldosteronsim?
Liddle syndrome pseudoaldosteronism is a genetic disorder characterized by early-onset hypertension, low potassium levels, metabolic alkalosis, and a family history of similar symptoms.
Who is required to file liddle syndrome pseudoaldosteronsim?
Individuals diagnosed with liddle syndrome pseudoaldosteronism or their healthcare providers may be required to report the condition to relevant healthcare authorities.
How to fill out liddle syndrome pseudoaldosteronsim?
To fill out liddle syndrome pseudoaldosteronism, detailed information about the diagnosis, symptoms, treatment, and family history of the condition should be accurately documented and reported.
What is the purpose of liddle syndrome pseudoaldosteronsim?
The purpose of reporting liddle syndrome pseudoaldosteronism is to track and monitor cases of this rare genetic disorder, assess its prevalence, and provide appropriate medical care and support to affected individuals.
What information must be reported on liddle syndrome pseudoaldosteronsim?
Information such as the patient's diagnosis, symptoms, treatment regimen, family history, and any relevant genetic testing results must be reported when filing liddle syndrome pseudoaldosteronism.
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