Dermatologic Differential Diagnosis.pdf. - Famona Site

Epidermolytic hyperkeratosis (bullous congenital ichthyosiform
erythroderma) Rook p.1505–1507, 1998, Sixth Edition
Erythrokeratoderma variabilis BJD 152:1143–1148, 2005; Ped
Derm 19:285–292, 2002; AD 122:441–445, 1986
Familial dyskeratotic comedones JAAD 17:808–814, 1987
Fine scaling, keratosis pilaris, periorificial crusting, palmoplantar
hyperkeratosis, blistering JAAD 34:379–385, 1996
Fitzsimmons syndrome Clin Genet 23:329–335, 1983
Focal acral hyperkeratosis (acrokeratoelastoidosis with
elastorrhexis) (punctate keratoderma) – autosomal dominant;
Afro-Caribbeans; umbilicated punctae at margins of palms and
soles Hautarzt 50:586–589, 1999; BJD 109:97–103, 1983
Focal palmoplantar and oral mucosa (gingival) hyperkeratosis
syndrome (MIM:148730) (hereditary painful callosities) –
palmoplantar keratoderma, leukoplakia (gingival keratosis), and
cutaneous horn of the lips JAAD 52:403–409, 2005; BJD
146:680–683, 2002; Oral Surg 50:250, 1980; Birth Defects
12:239–242, 1976; Arch Int Med 113:866–871, 1964
Focal palmoplantar keratoderma and sensorineural deafness
BJD 143:876–883, 2000
Gamborg–Nielsen (Norbotten type) palmoplantar keratoderma –
autosomal dominant; diffuse with papular border Clin Genet
28:361–366, 1985; autosomal recessive Dermatology
188:194–199, 1994; Arch Dermatol Res 282:363–370, 1990
Greither’s syndrome – poikiloderma of face and extremities;
warty keratoses over hands, feet, and legs; plantar
keratoderma; normal nails and hair Hautarzt 9:364–369, 1958
Greither’s palmoplantar keratoderma (transgrediens et
progrediens palmoplantar keratoderma) – hyperkeratoses
extending over Achilles tendon, backs of hands, elbows, knees;
livid erythema at margins JAAD 53:S225–230, 2005; Ped Derm
20:272–275, 2003; Cutis 65:141–145, 2000
Haim–Munk syndrome (same as Papillon–Lefevre syndrome
plus acro-osteolysis, acrachnodactyly, and pes planus) –
congenital palmoplantar keratoderma, progressive periodontal
destruction, recurrent skin infections (bacterial), arachnodactyly,
claw-like deformity of terminal phalanges BJD 152:353–356,
2005; BJD 147:575–581, 2002; Eur J Hum Genet 5:156–160,
1997
Hereditary acrokeratotic poikiloderma – papular keratotic
lesions of dorsae of hands AD 103:405–422, 1971
Hereditary callosities with blisters JAAD 11:409–415, 1984
Hereditary diffuse PPK with progressive neurosensory deafness
AD 118:605–607, 1982; J Laryngol Otol 89:1143–1146, 1975
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 PPK, type papulosa JAAD 29:435–437, 1993
Hereditary palmoplantar keratoderma, congenital alopecia,
onychodystrophy, enamel dysplasia Hautarzt 25:8–16, 1970
Hereditary PPK with leukoencephalopathy Neurology
45:331–337, 1995
Hereditary keratoderma, nail dystrophy, and hereditary motor
and sensory neuropathy – autosomal dominant J Med Genet
25:754–757, 1988
Hereditary reactive papulotranslucent acrokeratoderma
(punctate keratoderma) Australas J Dermatol 41:172–174,
2000; Cutis 61:29–30, 1998; JAAD 34:686–687, 1996
Hereditary punctate keratoderma and internal malignancy
JAAD 10:587–591, 1984
Hidrotic ectodermal dysplasia (Fischer–Jacobson–Clouston
syndrome) TIG 13:229, 1997
PALMOPLANTAR KERATODERMAS 437
HOPP syndrome – hypotrichosis, striate, reticulated pitted
palmoplantar keratoderma, acro-osteolysis, psoriasiform
plaques, lingua plicata, onychogryphosis, ventricular
arrhythmias, periodontitis BJD 150:1032–1033, 2004; BJD
147:575–581, 2002
Howell–Evans syndrome (tylosis) – autosomal dominant; focal
PPK; follicular prominence, oral leukokeratosis, carcinoma of
the esophagus Curr Prob Derm 14:71–116, 2002; Eur J Cancer
Oral Oncol 30:102–112, 1994; Q J Med 155:317–333, 1970;
QJMed 27:413–429, 1958; QJ Med 27:415–429, 1950
Huriez syndrome – palmoplantar keratoderma with
sclerodactyly TIG 13:229, 1997
Hyperkeratosis-hyperpigmentation syndrome TIG 13:229, 1997
Hypopigmentation with punctate keratoderma
Ichthyosis hystrix, Curth-Macklin type AD 141:779–784, 2005;
Am J Hum Genet 6:371–382, 1954
Ichthyosis vulgaris palmaris et plantaris dominans – form of
ichthyosis vulgaris Dermatologica 165:627–635, 1982
Keratoderma with scleroatrophy of the extremities (Huriez
syndrome) – autosomal dominant; diffuse keratoderma;
atrophic parchment-like skin over dorsal surface of hands;
pseudosclerodermatous appearance of hands
JAAD 26:855–857, 1992; Sem Hop Paris 44:481–488, 1968
Keratoderma with mental retardation and spastic paraplegia –
striate keratoderma of palms, diffuse keratoderma of the soles,
pes cavus, X-linked Clin Genet 23:329–335, 1983
Keratoderma with skeletal deformity (circumscribed) –
autosomal recessive
Keratoderma, woolly hair, follicular keratoses, blistering
Retinoids Today Tomorrow 37:15–19, 1994
Keratodermia maculosa disseminata symmetrica palmaris
et plantaris (punctate keratoderma)
Keratoma dissipatum hereditarium palmare et plantare (Brauer)
(punctate keratoderma)
Keratosis follicularis spinulosa decalvans JAAD 47:S275–278,
2002
Keratosis lichenoides chronica AD 131:609–614, 1995;
AD 105:739–743, 1972; JAAD 37:263–264, 1997; JAAD
38:306–309, 1998; Presse Med 46:1000, 1938
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
Keratosis multiformis – warty palmoplantar keratoderma;
atrophic skin over dorsal hands and feet, follicular keratoses,
punctate pigmentation of neck, forearms, buttocks; skeletal
abnormalities Arch Klin Exp Dermatol 209:243–257, 1959
Keratosis palmoplantaris nummularis (hereditary painful
callosities) (punctate keratoderma) – autosomal dominant; form
of epidermolytic hyperkeratosis; nummular keratoses on plantar
pressure points; painful; appears when child starts to walk
Dermatology 193:47–49, 1996; Acta DV 75:405–406, 1995;
JAAD 9:204–209, 1983; JAAD 25:113–114, 1991; AD
114:591–592, 1978
Keratosis palmoplantaris with periodontitis, pes planus, and
onychogryphosis, arachnodactyly, and acro-osteolysis BJD
115:243–248, 1986
Keratosis palmoplantaris papulosa seu maculosa (punctate
keratoderma)
Keratosis punctata of the palmar creases – autosomal dominant
disorder of African–Americans Rook p.3248, 1998, Sixth
Edition; Cutis 32:75–76, 1983; AD 116:669–671, 1980