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GlossaryKeratosis Follicularis Spinulosa Decalvans (KFSD)

rare genetic disorder causing rough skin and permanent hair loss

Keratosis Follicularis Spinulosa Decalvans (KFSD) is a rare genetic skin disorder characterized by the development of rough, spiny papules around hair follicles, leading to scarring and permanent hair loss (alopecia). It typically begins in childhood and can affect the scalp, eyebrows, and other body areas, often accompanied by redness and inflammation.

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research Keratosis Follicularis Spinulosa Decalvans

54 citations, January 1983 in “Archives of Dermatology”

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

research Keratosis Follicularis Spinulosa Decalvans: A Family Study of Seven Male Cases and Six Female Carriers

41 citations, January 1992 in “Journal of medical genetics”

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

research Keratosis Follicularis Spinulosa Decalvans in a Family

32 citations, February 2008 in “Journal of the American Academy of Dermatology”

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

research Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation

1 citations, January 2015 in “Journal of clinical case reports”

KFSD causes scarring hair loss and skin roughness, mainly in males.

research Common Causes of Hair Loss: Clinical Manifestations, Trichoscopy, and Therapy

47 citations, December 2020 in “Journal of the European Academy of Dermatology and Venereology”

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

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