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Keratosis pilaris atrophicans

rare

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

Identifiers: MONDO:0018855 OMIM:604093 Orphanet:498
Causal genes: LRP1
Part of: Epidermal disease Hereditary skin disorder Keratosis pilaris
Also known as: amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2 · Atrophodermia reticulata · Atrophodermia reticulata symmetrica faciei · Atrophodermia vermiculata · burnett Schwartz Berberian syndrome

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Keratosis follicularis spinulosa decalvans	MONDO:0000136	2
Atrophoderma vermiculata	MONDO:0008849
Keratosis pilaris atrophicans faciei	MONDO:0859588
Ulerythema ophryogenesis	MONDO:0018086

Rare disease

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