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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Xp22.3 deletions in isolated familial Kallmann's syndrome.

Several familial cases of Kallmann's syndrome (KS) have been reported, among which the X-chromosome-linked mode of inheritance is the most frequent. The gene responsible for the X-linked KS has been localized to the terminal part of the X-chromosome short arm (Xp22.3 region), immediately proximal to the steroid sulfatase gene responsible for X-linked ichthyosis. Large deletions of this region have been previously shown in patients affected with both X-linked ichthyosis and KS. We report here the search for Xp22.3 deletions in 20 unrelated males affected with isolated X-linked KS. Only 2 deletions were found using Southern blot analysis, indicating that large deletions are uncommon in patients affected with KS alone. Both deletions were shown to include the entire KAL gene responsible for X-linked KS. The patients carrying these deletions exhibit additional clinical anomalies, which are discussed: unilateral renal aplasia, unilateral absence of vas deferens, mirror movements, and sensory neural hearing loss.[1]

References

  1. Xp22.3 deletions in isolated familial Kallmann's syndrome. Hardelin, J.P., Levilliers, J., Young, J., Pholsena, M., Legouis, R., Kirk, J., Bouloux, P., Petit, C., Schaison, G. J. Clin. Endocrinol. Metab. (1993) [Pubmed]
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