Schneiderman Prelims Vol-I. qxd

Parthenon; p.xvi, 2000
Psoriasis, including rupioid psoriasis of feet
Reactive perforating collagenosis
Symmetrical interdigital hyperkeratosis of the hands
Acta DV 73:459–460, 1993
Terra firme (Diogenes syndrome) 
Lancet i:366–368, 1975
Transient reactive papulotranslucent acrokeratoderma 
Australas
J Dermatol 41:172–174, 2000
SYNDROMES
Apert’s syndrome – circumferential nail at tip of fused digits
Textbook of Neonatal Dermatology, p.509, 2001
Bannayan–Riley–Ruvalcaba–Zonana syndrome (PTEN
phosphatase and tensin homolog hamartoma) – acral
keratoses; facial verrrucous papules, angiokeratomas;
dolicocephaly, frontal bossing, macrocephaly, ocular
hypertelorism, long philtrum, thin upper lip, broad mouth,
relative micrognathia, lipomas, penile or vulvar lentigines, facial
verruca-like or acanthosis nigricans-like papules, multiple
acrochordons, angiokeratomas, transverse palmar crease,
accessory nipple, syndactyly, brachydactyly, vascular
malformations, arteriovenous malformations,
lymphangiokeratoma, goiter, hamartomatous intestinal
polyposis 
JAAD 53:639–643, 2005;
AD 132:1214–1218, 1996
Congenital malalignment of the great toenail – thickened nails
Rook p.2865, 1998, Sixth Edition
Corneal changes, hyperkeratosis, short stature, brachydactyly,
premature birth – autosomal dominant 
Am J Med Genet
18:67–77, 1984
Costello syndrome – warty papules around nose and
mouth, legs, perianal skin; loose skin of neck, hands, and feet,
thick palmoplantar surfaces, hypoplastic nails, short stature,
craniofacial abnormalities 
Eur J Dermatol 9:533–536, 1999;
Aust Paediat J 13:114–118, 1977
Cowden’s disease
Darier’s disease, including thickened nails 
Rook p.2865, 1998,
Sixth Edition
Deletion of long arm of chromosome 6 – circumferential nail
Textbook of Neonatal Dermatology, p.509, 2001
Dowling–Degos syndrome (reticulated pigmented anomaly of
the flexures) – seborrheic keratosis-like lesions 
BJD
147:568–571, 2002
Dyskeratosis benigna intraepithelialis mucosae et cutis
hereditaria – conjunctivitis, umbilicated keratotic nodules of
scrotum, buttocks, trunk; palmoplantar verruca-like lesions,
leukoplakia of buccal mucosa, hypertrophic gingivitis, tooth loss
J Cutan Pathol 5:105–115, 1978
Ectodermal defects – including thickened nails 
Rook p.2865,
1998, Sixth Edition
Epidermodysplasia verruciformis – spiny hyperkeratosis of
palms and soles 
Ped Derm 20:176–178, 2003; Int J Derm
37:766–771, 1998
Haim–Munk syndrome – autosomal recessive; mutation in
cathepsin C gene (like Papillon–Lefevre syndrome);
palmoplantar keratoderma, scaly red patches on elbows, knees,
forearms, shins, atrophic nails, gingivitis with destruction of
periodontium, onychogryphosis, arachnodactyly, recurrent
pyogenic infections 
BJD 152:353–356, 2005
Hereditary (bullous) acrokeratotic poikiloderma of Weary
(acrokeratotic poikiloderma) (Kindler’s syndrome?) – autosomal
dominant – vesiculopustular eruption of hands and feet in
infancy and childhood; extensive dermatitis in childhood,
persistent poikiloderma sparing face, scalp and ears, verrucous
papules of hands, feet, elbows, and knees 
AD 103:409–422,
1971; pseudoainhum and sclerotic bands Int J Dermatol
36:529–533, 1997; AD 103:409–422, 1971
Hereditary callosities – blisters at periphery of calluses
JAAD 11:409–415, 1984
Hereditary focal transgressive palmoplantar keratoderma –
autosomal recessive; hyperkeratotic lichenoid papules of elbows
and knees, psoriasiform lesions of scalp and groin, spotty and
reticulate hyperpigmentation of face, trunk, and extremities,
alopecia of eyebrows and eyelashes 
BJD 146:490–494, 2002
Hereditary sensory and autonomic neuropathy type I – calluses
over metatarsal heads which blister, necrose, and ulcerate
Rook p.2779, 1998, Sixth Edition
Hystrix-like ichthyosis–deafness syndrome – postnatal
erythroderma, generalized spiky and cobblestoned