Keratosis follicularis spinulosa decalvans: Difference between revisions
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==Overview== | ==Overview== | ||
'''Keratosis follicularis spinulosa decalvans''' (also known as "Siemens-1 syndrome") is a rare X-linked disorder described by [[Hermann Werner Siemens|Siemens]] in 1926, a disease that begins in infancy with [[keratosis pilaris]] localized on the face, then evolves to more diffuse involvement.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0721629210.</ref>{{rp|580,762}}<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0071380760.</ref>{{rp|649,714}} | '''Keratosis follicularis spinulosa decalvans''' (also known as "Siemens-1 syndrome") is a rare X-linked disorder described by [[Hermann Werner Siemens|Siemens]] in 1926, a disease that begins in infancy with [[keratosis pilaris]] localized on the face, then evolves to more diffuse involvement.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0721629210.</ref>{{rp|580,762}}<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0071380760.</ref>{{rp|649,714}} | ||
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== References == | == References == | ||
{{reflist}} | {{reflist|2}} | ||
[[Category:Genodermatoses]] | [[Category:Genodermatoses]] | ||
Latest revision as of 18:54, 4 September 2012
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| OMIM | 308800 |
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Overview
Keratosis follicularis spinulosa decalvans (also known as "Siemens-1 syndrome") is a rare X-linked disorder described by Siemens in 1926, a disease that begins in infancy with keratosis pilaris localized on the face, then evolves to more diffuse involvement.[1]:580,762[2]:649,714