has material basis in germline mutation in LRP1 keratosis pilaris atrophicans https://rarediseases.info.nih.gov/diseases/1042/burnett-schwartz-berberian-syndrome https://www.malacards.org/card/keratosis_pilaris_atrophicans MESH:C537412 keratosis pilaris atrophicans folliculitis ulerythematosa amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2 MEDGEN:75520 keratosis pilaris atrophicans facies ulerythema ophryogenes with multiple congenital anomalies icd11.foundation:273325594 ulerythema ophryogenes Orphanet:498 ulerythema ophryogenesis KPA An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair. SCTID:400059005 UMLS:C0263428 Atrophodermia reticulata symmetrica faciei Atrophodermia vermiculata MONDO:0018855 Atrophodermia reticulata folliculitis ulerythematosa reticulata GARD:0018694 DOID:0080751 keratosis pilaris honeycomb atrophy ICD9:757.39 burnett Schwartz Berberian syndrome OMIM:604093 epidermal disease keratosis pilaris hereditary skin disorder