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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 Unilateral Keratosis Pilaris Atrophicans Faciei Mimicking Follicular Mucinosis

3 citations , April 2011 in “Journal of the American Academy of Dermatology”

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

research Keratosis Follicularis Spinulosa Decalvans Associated With Acne Keloidalis Nuchae And Tufted Hair Folliculitis

35 citations , January 2008 in “American Journal of Clinical Dermatology”

KFSD can be linked to acne keloidalis nuchae and tufted hair folliculitis.

research A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child

January 2022 in “Clinical dermatology review”

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

research Keratosis Follicularis Spinulosa Decalvans: What Syndrome Is This?

5 citations , March 2005 in “Pediatric dermatology”

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

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.

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