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Keratosis pilaris atrophicans

MONDO:0018855

An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair.

Also known as: keratosis pilaris atrophicans, Atrophodermia reticulata, Atrophodermia reticulata symmetrica faciei, Atrophodermia vermiculata, KPA, amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2, burnett Schwartz Berberian syndrome, folliculitis ulerythematosa

8 clinical trials for this condition and its sub-types.

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Sub-types

Atrophoderma vermiculata (0) Keratosis follicularis spinulosa decalvans (0) Keratosis follicularis spinulosa decalvans, autosomal dominant (0) Keratosis follicularis spinulosa decalvans, X-linked (0) Keratosis pilaris atrophicans faciei (0) Ulerythema ophryogenesis (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Keratosis pilaris (1) Disease by body system or component (0) Disease by etiologic mechanism (0) Epidermal disease (0)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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