Department of Dermatology, St. John's Medical College and Hospital, Koramangala, Bangalore, Karnataka-560 034, India.
Indian J Dermatol Venereol Leprol. 2011 May-Jun;77(3):325-7. doi: 10.4103/0378-6323.79708.
Keratosis follicularis spinulosa decalvans (KFSD), is a rare follicular syndrome associated with widespread keratosis pilaris and progressive scarring alopecia. This genodermatoses often starts at infancy or early childhood with an X-linked mode of inheritance. Males are predominantly affected and females frequently show no disease or only a mild form. We describe this not so common entity of KFSD in a nine year old female child.
遗传性脱发性棘状毛囊角化病(KFSD)是一种罕见的毛囊综合征,伴有广泛的毛发角化病和进行性瘢痕性脱发。这种遗传性皮肤病常始于婴儿期或幼儿期,呈 X 连锁遗传模式。男性受影响更为严重,而女性通常无病或仅有轻度表现。我们在一名 9 岁女童中描述了这种不那么常见的 KFSD 病例。