Keratosis follicularis spinulosa decalvans

Also Known As:
Keratosis follicularis spinulosa decalvans cum ophiasi
Networked: 29 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results


1. Grzeschik, Karl-Heinz: 2 articles (04/2013 - 10/2010)
2. Bornholdt, Dorothea: 2 articles (04/2013 - 10/2010)
3. Castori, Marco: 2 articles (11/2010 - 01/2009)
4. Sacchidanand, S: 1 article (07/2015)
5. Malvankar, Dipali D: 1 article (07/2015)
6. Pirmez, Rodrigo: 1 article (11/2014)
7. Ramos-e-Silva, Marcia: 1 article (11/2014)
8. Wang, H J: 1 article (03/2014)
9. Dai, L L: 1 article (03/2014)
10. Tang, Z L: 1 article (03/2014)

Related Diseases

1. Alopecia (Baldness)
2. Cicatrix (Scar)
3. Photophobia (Light Sensitivity)
4. Ichthyosis (Xeroderma)
01/01/1987 - "This kindred has features of both keratosis follicularis spinulosa decalvans and ichthyosis follicularis, and the disorder seems to fit into the group of follicular hyperkeratosis disorders."
01/01/1985 - "Keratosis follicularis spinulosa decalvans (ichthyosis follicularis or Siemens's syndrome) is considered a general form of keratosis pilaris decalvans. "
04/01/2013 - "Missense mutations affecting membrane-bound transcription factor protease site 2 (MBTPS2) have been associated with Ichthyosis Follicularis with Atrichia and Photophobia (IFAP) syndrome with or without BRESHECK syndrome, with keratosis follicularis spinulosa decalvans, and Olmsted syndrome. "
09/01/1985 - "This disorder must be differentiated from keratosis follicularis spinulosa decalvans; ulerythema ophryogenes; keratosis pilaris rubra atrophicans faciei; atrichia with papular lesions; atrophodermia vermiculata; and keratitis, ichthyosis, and deafness syndrome, all of which share some clinical features. "
03/01/2014 - "Mutations in MBTPS2 have been reported to cause a broad phenotypic spectrum of X-linked genodermatoses, including IFAP (ichthyosis follicularis; atrichia and photophobia) syndrome (OMIM 308205) with or without BRESHECK (brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia) syndrome, keratosis follicularis spinulosa decalvans (KFSD; OMIM 308800) and an X-linked form of Olmsted syndrome. "
5. Acne Keloid (Acne Keloidalis)

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