Schneiderman Prelims Vol-I. qxd

AUTOIMMUNE DISEASES, AND DISEASES OF
IMMUNE DYSFUNCTION
Adult Still’s disease – palmoplantar vesiculopustular eruption
with fixed facial papules 
J Korean Med Sci 17:852–855, 2002
Allergic contact dermatitis – granulomatous allergic contact
dermatitis due to topical propolis 
BJD 144:1277–1278, 2001
Bowel-associated dermatitis-arthritis syndrome 
AD
135:1409–1414, 1999
Chronic granulomatous disease – translucent facial papules
around eyes, nose, lips, cheeks; mimics lupus vulgaris 
NEJM
317:687–694, 1987
Dermatitis herpetiformis 
Dermatologica 155:350–354, 1977
Hyper-IgE syndrome – papulopustules of face and scalp in first
year of life 
J Pediatr 141:572–575, 2003; Clin Exp Dermatol
11:403–408, 1986; Medicine 62:195–208, 1983
Lupus erythematosus – arteritis, lupus profundus 
JAAD
16:839–844, 1987, discoid lupus, systemic lupus;
chilblain lupus – red papules of face, nose 
Cutis
69:183–184,190, 2002; tumid lupus
Urticaria
CONGENITAL
Accessory tragus – facial, glabellar papule – isolated 
Textbook
of Neonatal Dermatology, p.118, 2001; Goldenhaar syndrome
Accessory tragi 
JAAD 50:S11–13, 2004
Delleman syndrome – autosomal dominant with variable
penetrance, orbital cysts (exophthalmia or microthalmia),
cerebral malformations, periorbital or postauricular
appendages, focal dermal hypoplasia and aplasia, rib defects,
psychomotor retardation, seizures, skull defects
Goldenhaar syndrome – (oculo-auriculo-vertebral
syndrome) – macroglossia, preauricular tags, abnormal
pinnae, facial asymmetry, macrostomia, epibulbar dermoids,
facial weakness, central nervous system, renal, and skeletal
anomalies),
Hurson syndrome
Nagers syndrome
Treacher Collins syndrome (mandibulofacial dysostosis –
autosomal dominant; auricular defects, malar hypoplasia,
down-slanting palpebral fissures, lower eyelid defects
Townes–Brocks syndrome – autosomal dominant; external
ear malformations, polydactyly, renal and anal malformations
Am J Med Genet 18:147–152, 1984