Schneiderman Prelims Vol-I. qxd

PSYCHOCUTANEOUS DISEASES
Factitial traumatic panniculitis mimicking acrodermatitis
atrophicans 
JAAD 13:988–994, 1985
Neurotic excoriations – atrophic scars 
Compr Psychiatry
27:381–386, 1986
SYNDROMES
Achenbach’s syndrome (paroxysmal hematoma of the finger) –
mimics bruising or steroid atrophy 
Rook p.2007, 1998,
Sixth Edition; BJD 132:319, 1995
Acquired partial lipodystrophy (progressive lipodystrophy, partial
lipodystrophy, Barraquer–Simons syndrome) – gradual-onset loss
of subcutaneous fat from face, neck, trunk, and upper extremities
during childhood; normal or excess amount of subcutaneous fat
in hips and lower extremities, proteinuria or mesangiocapillary
glomerulonephritis, low C3, presence of C3-nephritic factor, no
insulin resistance; presence of other autoimmune diseases 
J Clin
Endocrinol Metab 85:1776–1782, 2000
Acrocephalopolysyndactyly
Acrogeria – atrophy and mottled hyperpigmentation of acral
skin; thick or thin nails, micrognathia, atrophic tip of nose
BJD 151:497–501, 2004; BJD 142:178–180, 2000; BJD
103:213–223, 1980; Arch Dermatol Syphiligr 181:571–583, 1941
Adams–Oliver syndrome – congenital scalp ACC and amniotic
bands with reduction of terminal phalanges of fingers and toes
(terminal transverse limb defects) 
Textbook of Neonatal
Dermatology, p.127, 2001; Clin Genet 47:80–84, 1995; J Hered
36:3–7, 1945
Amniotic band syndrome 
Int J Dermatol 27:312–4, 1988
Anhidrotic ectodermal dysplasia
Anonychia with ectrodactyly
AREDYLD syndrome – ectodermal dysplasia, lipoatrophy,
diabetes, mellitus, amastia 
Am J Med Genet 44:374–377,
1992; Am J Med Genet 16:29–33, 1983
Ascher’s syndrome – periorbital edema; edema of lips,
double lip, blepharochalasis 
AD 139:1075–1080, 2003;
Rook p.2984, 1998, Sixth Edition; Klin Monatsbl Augenheilkd
65:86–97, 1920
Ataxia telangiectasia – lipoatrophy 
JAAD 42:939–969, 2000;
JAAD 10:431–438, 1984; atrophic plaque of cutaneous
granuloma of ataxia telangiectasia 
AD 134:1145–1150,
1998; atrophy of skin Rook p.2095, 1998, Sixth Edition
Baraitser syndrome (premature aging with short stature and
pigmented nevi) – lack of facial subcutaneous fat, fine hair,
hypospadias, dental abnormalities, hepatomegaly 
J Med
Genet 25:53–56, 1988
Barber–Say syndrome – autosomal dominant or X-linked;
macrostomia, hypertelorism, atrophic skin, hypertrichosis
Am J Med Genet 73:366–367, 1997
Bart’s syndrome – aplasia cutis congenita of the legs with
dystrophic epidermolysis bullosa 
Caputo p.131, 2000
Bazex–Dupre–Christol syndrome (X-linked dominant) – milia
and comedo-like papules, congenital hypotrichosis, anhidrosis,
X-linked dominant, follicular (vermiculate) atrophoderma of the
face, elbows and hands, hypohidrosis, basal cell nevi and basal
cell carcinomas, pinched nose, keratosis pilaris, scrotal tongue,
joint hypermobility 
BJD 153:682–684, 2005; Dermatol Surg
26:152–154, 2000; Ped Derm 16:108–110, 1999; JAAD
39:853–857, 1998; AD 130:337–342, 1994; Hautarzt
44:385–391, 1993; Ann Dermatol Syphilgr (Paris) 93:241–254,
1966; Bull Soc Franc Derm Syph 71:206,1964
Beckwith–Wiedemann syndrome (exomphalos–macroglossia–
gigantism) (EMG) syndrome – autosomal dominant; zosteriform
rash at birth, circular depressions of helices, exomphalos,
macroglossia, visceromegaly, facial nevus flammeus and
gigantism; earlobe grooves, punched-out depressions of
posterior pinna 
JAAD 37:523–549, 1997; Am J Dis Child
122:515–519, 1971
Bencze syndrome – hemifacial atrophy with esotropia,
amblyopia, and submucous cleft palate 
Clin Genet
16:301–304, 1979