Schneiderman Prelims Vol-I. qxd

ICHTHYOSIFORM ERUPTIONS: ACQUIRED ICHTHYOSIS
287
Schneiderman page 200-300.qxd 5/16/2006 6:49 PM Page 287

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Ichthyosis exfoliativa – autosomal recessive; peeling of
neonate; resembles ichthyosis bullosa of Siemens in adult life
BJD 149:174–180, 2003; thought to be identical to ichthyosis
bullosa of Siemens 
JAAD 27:348–355, 1992; BJD
124:191–194, 1991
Ichthyosis hystrix (Curth–Macklin) – autosomal dominant; spiky
hyperkeratosis; epidermolytic hyperkeratosis with diffuse or
striate PPK 
Curr Prob Derm 14:71–116, 2002; Rook p.1510,
1998, Sixth Edition
Ichthyosis with renal disease – red skin, fine scale, vesicles over
dorsal hands and feet, aminoaciduria, dwarfism, mental
retardation 
J Pediatr 82:466–470, 1973
Ichthyosis, mental retardation, dwarfism, and renal impairment
J Pediatr 92:766–768, 1978
Ichthyosis, split hairs, aminoaciduria
Ichthyosis variegata (congenital reticular ichthyosiform
erythroderma) 
BJD 139:893–896, 1998
Ichthyosis vulgaris – autosomal dominant; fine white scale 
Curr
Prob Derm 14:71–116, 2002; Rook p.1487, 1998, Sixth Edition
Ichthyosis vulgaris-like with keratoderma and increased serum
β
-glucuronidase 
Dermatologica 177:341–347, 1988
Ichthyosis vulgaris-like – autosomal recessive; no collodion
membrane 
AD 122:428–433, 1986
Ichthyosis vulgaris palmaris et plantaris dominans
Dermatologica 165:627–635, 1982
Lamellar ichthyosis – autosomal recessive 
Rook p.1500–1501,
1998, Sixth Edition; autosomal dominant Clin Genet
30:122–126, 1986; Clin Genet 26:457–461, 1984
Loricrin keratoderma – ichthyosis, palmoplantar keratoderma,
pseudoainhum 
Ped Derm 19:285–292, 2002
Non-bullous CIE (congenital ichthyosiform erythroderma)
(erythrodermic lamellar ichthyosis) – autosomal recessive;
collodion baby; fine white scales, background erythema
Curr Prob Derm 14:71–116, 2002; AD 121:477–488, 1985
Pityriasis rotunda – may be paraneoplastic phenomenon; or
with leprosy 
JAAD 31:866–871, 1994; JAAD 14:74–78, 1986;
BJD 76:223–227, 1964
Progressive symmetric erythrokeratoderma 
Textbook
of Neonatal Dermatology, p.287, 2001
X-linked recessive ichthyosis (steroid sulfatase deficiency) –
large dark scaling of extensor surfaces of outer arms, outer
thighs, around lower legs; flexures may be involved 
Curr Prob
Derm 14:71–116, 2002; Br Med J 1:947–950, 1966
X-linked recessive ichthyosis (multiple sulfatase deficiency) –
combination of mucopolysacchariosis type 2 (aryl sulfatase
B deficiency), metachromatic leukodystrophy (aryl sulfatase
A deficiency), and XLRI 
Ped Derm 14:369–372, 1997;
Clin Genet 30:409–415, 1986
X-linked recessive ichthyosis without steroid sulfatase
deficiency 
Am J Med Genet 59:143–148, 1995