Schneiderman Prelims Vol-I. qxd

SYNDROMES
Annular epidermolytic ichthyosis – variant of bullous congenital
ichthyosiform erythroderma – mutation in keratin 10 
JID
111:1220–1223, 1998
CHILD syndrome (hemidysplasia, ichthyosiform erythroderma,
unilateral limb defects (hypoplasia)) – X-linked dominant;
unilateral inflammatory epidermal nevus or unilateral
ichthyosiform erythroderma with skeletal abnormalities 
AD
123:503–509, 1987
Congenital reticular ichthyosiform erythroderma (ichthyosis
variegata, ichthyosis en cocarde) 
BJD 139:893–896, 1998;
Dermatology 188:40–45, 1994
Conradi–Hünermann syndrome – generalized erythema 
Hum
Genet 53:65–73, 1979
Degos’ syndrome – erythrokeratodermia en cocardes
Degos–Touraine syndrome – incontinentia pigmenti with
poikiloderma in photodistribution, bullae of face, extremities;
chronic erythroderma with subsequent hyperpigmentation 
Soc
Gr Dermatol Syph 68:6–10, 1961
Dermatitis–eosinophilia syndrome following wasp sting 
AD
120:1595–1597, 1984
Happle’s syndrome – X-linked dominant chondrodysplasia
punctata 
Ped Derm 13:1–4, 1996
Hypereosinophilic syndrome 
Ped Derm 15:363–371, 1996;
Semin Dermatol 14:122–128, 1995; Blood 83:2759–2779, 1994;
in AIDS 
JAAD 23:202–204, 1990
Hystrix-like ichthyosis–deafness syndrome – postnatal
erythroderma, generalized spiky and cobblestoned
hyperkeratosis, sensorineural deafness, connexin mutation 
BJD
146:938–942, 2002
Ichthyosiform erythroderma and cardiomyopathy 
BJD
139:1055–1059, 1998
Ichythyosis bullosa of Siemens 
Clin Exp Derm 15:53–56, 1990
Ichthyosis congenita type IV – erythrodermic infant with follicular
hyperkeratosis 
BJD 136:377–379, 1997
Kawasaki’s disease
Keratosis linearis with ichthyosis and sclerosing keratoderma
(KLICK syndrome) – autosomal recessive; erythroderma,
palmoplantar keratoderma, ainhum, red elbows and knees
BJD
153:461, 2005; Acta DV 77:225–227, 1997; Am J Hum Genet
61:581–589, 1997
KID syndrome – keratosis, ichthyosis, deafness syndrome –
erythrokeratoderma-like 
Ped Derm 17:115–117, 2000; Ped
Derm 13:105–113, 1996
Leiner’s syndrome 
NEJM 282:354, 1976; J Ped 80:879, 1972
MAUIE syndrome – erythroderma with skip areas;
micropinnae, alopecia, ichthyosis, and ectropion 
JAAD
37:1000–1002, 1997
Netherton’s syndrome
AD 135:823–832, 1999; BJD
141:1097–1100, 1999; Ped Derm 14:473–476, 1997; Ped Derm
13:183–199, 1996
Neutral lipid storage disease (Dorfman–Chanarin syndrome) 
–
autosomal recessive; at birth collodion baby or ichthyosiform
erythroderma (non-bullous congenital ichthyosiform
erythroderma and neutral lipid storage disease); thereafter
pattern resembles non-bullous ichthyosiform erythroderma;
hypohidrosis; ectropion; palmoplantar hyperkeratosis, WBC
vacuoles, myopathy, fatty liver, CNS disease, deafness
AD 141:798–800, 2005; Am J Dermatopathol 20:79–85, 1998;
JAAD 17:801–808, 1987; AD 121:1000–1008, 1985
Omenn’s syndrome – autosomal recessive; immunodeficiency;
erythroderma with occasional alopecia of scalp and eyebrows;
generalized adenopathy with hepatosplenomegaly 
Ped Derm
14:49–52, 1997; JAAD 25:442–446, 1991
Phakomatosis pigmentovascularis
Progressive symmetric erythrokeratoderma – autosomal
dominant; hyperkeratotic patches 
Curr Prob Derm 14:71–116,
2002
Red man syndrome (idiopathic) 
JAAD 18:1307, 1988
Reiter’s syndrome 
Rook p.2765–2766, 1998; Semin Arthritis
Rheum 3:253–286, 1974
Restrictive dermopathy – autosomal recessive 
Textbook of
Neonatal Dermatology, p.139,289, 2001
Tay syndrome – collodion baby 
Pediatrics 87:571–574, 1991
Vogt–Koyanagi–Harada disease – prodrome erythroderma
Dermatology 198:65–68, 1999