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Non-Invasive Imaging Techniques (Dermoscopy, Reflectance Confocal Microscopy and Line-Field Confocal Optical Coherence Tomography) for the Diagnosis of Warty Dyskeratoma. [PDF]
Cortonesi G +5 more
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Lichen planopilaris in children: Clinical characteristics, comorbidities, and treatment outcomes in a single-center case series. [PDF]
Lawrence CN +6 more
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Keratosis Follicularis Spinulosa (Lichen Spinulosus) in a Girl, aged 8.
Dore Se
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Comorbidities in primary cicatricial alopecia: a systematic review and meta-analysis. [PDF]
Yongpisarn T, Tejapira K, Suchonwanit P.
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Increased caries risk in a Xerostomic patient with Darier disease: a case report of incipient and advanced carious lesions. [PDF]
Giannakopoulos K +3 more
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Keratosis follicularis spinulosa decalvans.
European Journal of Pediatric Dermatology, 2018Keratosis follicularis spinulosa decalvans is a dominant X-linked hereditary disorder thus affecting less severely females, but it can be autosomal dominant or more often sporadic. Its boundaries with other forms of keratosis follicularis atrophicans are not clear and there is overlapping with other diseases included in the group of lichen planopilaris,
P. Chieco
openaire +2 more sources
Journal of dermatology (Print), 2023
Keratosis follicularis spinulosa decalvans (KFSD) is a rare X‐linked hereditary disorder characterized by the triad of follicular hyperkeratosis‐photophobia‐alopecia. The clinical heterogeneity makes the diagnosis difficult.
Xuemei Lan +8 more
semanticscholar +1 more source
Keratosis follicularis spinulosa decalvans (KFSD) is a rare X‐linked hereditary disorder characterized by the triad of follicular hyperkeratosis‐photophobia‐alopecia. The clinical heterogeneity makes the diagnosis difficult.
Xuemei Lan +8 more
semanticscholar +1 more source

