Schneiderman Prelims Vol-I. qxd

Parthenon; p.120, 2000
Lichen simplex chronicus – psoriasiform neurodermatitis
BJD 138:921–922, 1998
Lipedematous alopecia – boggy scalp with diffuse alopecia
JAAD 52:152–156, 2005; AD Syphilol 32:688, 1935
Pityriasis rubra pilaris 
J Dermatol 27:174–177, 2000;
JAAD 31:997–999, 1994
Pityriasis capitis (dandruff) 
Rook p.2941, 1998, Sixth Edition
Pityriasis rubra pilaris, childhood form 
Ped Derm 4:21–23, 1987
Psoriasis 
Rook p.2940, 1998, Sixth Edition; AD 98:248–259,
1968; tinea amientacea Clin Exp Dermatol 2:137–143, 1977
Seborrheic dermatitis 
Dermatology 201:146–147, 2001; Textbook
of Neonatal Dermatology, p.247, 2001; tinea amientacea Cutis
63:169–170, 1999; Hautarzt 25:134–139, 1974
Terra firme
Tinea amientacea 
Clin Exp Dermatol 2:137–144, 1977
PSYCHOCUTANEOUS DISEASES
Factitial dermatitis – with underlying osteomyelitis of the scalp
Acta Neurochir (Wien) 143:737–738, 2001; with resultant
cerebral abscess 
Postgrad Med J 64:976–977, 1988
Neurotic excoriations 
The Clinical Management of Itching;
Parthenon; p.119, 2000
SYNDROMES
Andogsky syndrome – atopic dermatitis and unilateral cataracts
Ped Derm 20:419–420, 2003; Klin Monatsbl Augenheilkd
52:824–831, 1914
Ankyloblepharon, ectodermal dysplasia, and cleft lip and palate
syndrome (AEC syndrome) (Hay–Wells syndrome) – hair
sparse or absent, dystrophic nails, dystrophic widely spaced
pointed teeth are shed early, chronic scalp erosions (erosive
scalp dermatitis) in early childhood 
BJD 94:287–289, 1976; Ped
Derm 14:149–150, 1997
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Ectodermal dysplasias with clefting – scalp dermatitis 
JAAD
27:249–256, 1992
Ectrodactyly–ectodermal dysplasia–cleft lip/palate (EEC)
syndrome 
Dermatology 194:191–194, 1997; BJD 132:621–625,
1995; JAAD 29:505–506, 1993
Happle syndrome (X-linked chondrodysplasia punctata) – scalp
dermatitis at birth; Blaschko hyperkeratoses, follicular
atrophoderma, cicatricial alopecia 
Ped Derm 18:442–444, 2001
Hay–Wells syndrome (AEC syndrome)- erosions 
Ped Derm
10:334–340, 1993; AD 128:1378–1386, 1992; JAAD
12:810–815, 1985
Hyper-IgE syndrome (Job’s syndrome) (Buckley’s syndrome) –
papular, pustular, excoriated dermatitis of face, behind ears,
scalp, axillae, and groin; recurrent bacterial infections of skin
with cold abscesses, contact urticaria, infections of nasal
sinuses and respiratory tract; growth failure 
AD 140:1119–1125,
2004; J Pediatr 141:572–575, 2002; NEJM 340:692–702, 1999;
Curr Prob Derm 10:41–92, 1998; Clin Exp Dermatol
11:403–408, 1986; Medicine 62:195–208, 1983; Pediatrics
49:59–70, 1972; Lancet 1:1013–1015, 1966
Hypoplastic enamel–onycholysis–hypohidrosis
(Witkop–Brearley–Gentry syndrome) – marked facial
hypohidrosis, dry skin with keratosis pilaris, scaling and crusting
of the scalp, onycholysis and subungual hyperkeratosis,
hypoplastic enamel of teeth 
Oral Surg 39:71–86, 1975
Ichthyosis follicularis with atrichia and photophobia (IFAP) –
atopic dermatitis; collodion membrane and erythema at birth;
ichthyosis, spiny (keratotic) follicular papules (generalized
follicular keratoses), non-scarring alopecia, keratotic papules of
elbows, knees, fingers, extensor surfaces, xerosis; punctate
keratitis, photophobia; nail dystrophy, psychomotor delay, short
stature; enamel dysplasia, beefy red tongue and gingiva,
angular stomatitis, lamellar scales, psoriasiform plaques,
palmoplantar erythema 
Curr Prob Derm 14:71–116, 2002;
JAAD 46:S156–158, 2002; BJD 142:157–162, 2000; AD
125:103–106, 1989; Ped Derm 12:195, 1995; Dermatologica
177:341–347, 1988; Am J Med Genet 85:365–368, 1999
Keratosis–ichthyosis–deafness syndrome – hyperkeratotic
papules and plaques of face, scalp, trunk, extremities;
exaggerated diaper dermatitis 
Ped Derm 13:105–113, 1996;
BJD 122:689–697, 1990; psoriasiform scalp dermatitis
BJD 148:649–653, 2003
Netherton’s syndrome – flexural lichenification; trichorrhexis
invaginata 
Ped Derm 19:285–292, 2002; AD 135:823–832,
1999; BJD 141:1097–1100, 1999; Curr Prob Derm 10:41–92,
1998; Ped Derm 14:473–476, 1997; Ped Derm 13:183–199,
1996; BJD 131:615–619, 1994
Omenn’s syndrome 
Acta Derm 782:71, 1988; presents in
neonatal period with atopic-like dermatitis 
Textbook of Neonatal
Dermatology, p.255, 2001
Rapp–Hodgkin hypohidrotic ectodermal dysplasia – autosomal
dominant; alopecia of wide area of scalp in frontal to crown
area, short eyebrows and eyelashes, coarse wiry sparse
hypopigmented scalp hair, sparse body hair, scalp dermatitis,
ankyloblepharon, syndactyly, nipple anomalies, cleft lip and/or
palate; nails narrow and dystrophic, small stature, hypospadius,
conical teeth and anodontia or hypodontia; distinctive facies,
short stature 
JAAD 53:729–735, 2005; Ped Derm 14:149–150,
1997; Ped Derm 7:126–131, 1990; J Med Genet 15:269–272,
1968;
Schwachman’s syndrome – neutropenia, malabsorption, failure
to thrive; generalized xerosis, follicular hyperkeratosis,
widespread dermatitis, palmoplantar hyperkeratosis 
Ped Derm
9:57–61, 1992; Arch Dis Child 55:531–547, 1980; J Pediatr
65:645–663, 1964
Trichothiodystrophy syndromes – BIDS, IBIDS, PIBIDS –
dermatitis, sparse or absent eyelashes and eyebrows, brittle
hair, premature aging, sexual immaturity, ichthyosis,
dysmyelination, bird-like facies, dental caries;
trichothiodystrophy with ichthyosis, urologic malformations,
hypercalciuria and mental and physical retardation
JAAD 44:891–920, 2001; Ped Derm 14:441–445, 1997
Wiskott–Aldrich syndrome – dermatitis, thrombocytopenia,
malignant lymphoma, leukemia 
Curr Prob Derm 14:41–70,
2002; Textbook of Neonatal Dermatology, p.255, 2001; Rook
p.700,2746, 1998, Sixth Edition; Int J Dermatol 24:77–81, 1985
TRAUMA
Intrapartum internal fetal monitoring – infectious dermatitis
Pediatrics 74:81–85, 1984
Radiation dermatitis 
Neurosurgery 34:1105, 1994; BJD
138:799–805, 1998