Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2

Keratosis follicularis spinulosa decalvans (KFSD) is a rare, X linked disorder with skin and eye involvement (MIM 308800). We have studied a large British family with KFSD using polymorphic markers from Xp21-p23 and obtained a lod score of 2.056 at theta=0 with markers proximal and distal to the KFS...

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Veröffentlicht in:Journal of medical genetics 1998-04, Vol.35 (4), p.336-337
Hauptverfasser: Porteous, M E, Strain, L, Logie, L J, Herd, R M, Benton, E C
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Sprache:eng
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Zusammenfassung:Keratosis follicularis spinulosa decalvans (KFSD) is a rare, X linked disorder with skin and eye involvement (MIM 308800). We have studied a large British family with KFSD using polymorphic markers from Xp21-p23 and obtained a lod score of 2.056 at theta=0 with markers proximal and distal to the KFSD candidate region Xp22.13-p22.2 identified by Oosterwijk et al. Our data confirm the linkage to Xp22.13-p22.2 observed in the previously reported Dutch family, but fail to narrow the candidate interval for the KFSD locus.
ISSN:0022-2593
1468-6244
1468-6244
DOI:10.1136/jmg.35.4.336