Key result
Genetic analysis strongly links familial hyperaldosteronism type II to chromosome 7p22.
Population
Five families with familial hyperaldosteronism type II, including affected and unaffected individuals.
Design
Other
Authors
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Does not change FH-II management; confirms 7p22 linkage and leaves open causative variant identification.
Observational
Yes
Effect estimate: LOD score 5.22
This study confirms the linkage of familial hyperaldosteronism type II to chromosome 7p22 across multiple geographical regions, highlighting its importance for identifying the causative mutation.
Sukor et al. (2008) conducted an observational in Familial hyperaldosteronism type II. Chromosome 7p22 locus was evaluated on Combined multipoint logarithm of odds (LOD) score for linkage at 7p22 (LOD score 5.22). Genetic analysis of five families with familial hyperaldosteronism type II demonstrated highly significant linkage to chromosome 7p22 with a combined multipoint LOD score of 5.22.
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