Schneiderman Prelims Vol-I. qxd

592
A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Schneiderman page 500-600.qxd 5/16/2006 6:51 PM Page 592

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Hunter’s syndrome – decreased sulfoiduronate sulfatase 
Ped
Derm 15:370–373, 1998
Incontinentia pigmenti – hyper or hypopigmentation 
Ped Derm
7:174–178, 1990
Jackli syndrome – generalized reticulated hyperpigmentation
with alopecia, microdontia, and childhood cataracts
Keratosis lichenoides chronica (Nekam’s disease) – reticulated
hyperpigmented plaques 
JAAD 49:511–513, 2003; JAAD
38:306–309, 1998; AD 131:609–614, 1995
Keratosis–ichthyosis–deafness (KID) syndrome – reticulated
palmoplantar keratoderma; reticulated hyperkeratotic facial
lesion 
AD 123:777–782, 1987
Kindler’s syndrome – reticulate erythema 
AD 133:1111–1117,
1997; Ped Derm 13:397–402, 1996
Koraxitrachitic syndrome – self-healing collodion baby; heals
with mottled reticulated atrophy; alopecia, absent eyelashes and
eyebrows, conjunctival pannus, hypertelorism, prominent nasal
root, large mouth, micrognathia, brachydactyly, syndactyly of
interdigital spaces 
Am J Med Genet 86:454–458, 1999
Macrocephaly with cutis marmorata, hemangioma, and
syndactyly syndrome – macrocephaly, hypotonia,
hemihypertrophy, hemangioma, cutis marmorata telangiectatica
congenita, internal arteriovenous malformations, syndactyly,
joint laxity, hyperelastic skin, thickened subcutaneous tissue,
developmental delay, short stature, hydroocephalus 
Ped Derm
16:235–237, 1999
MELAS syndrome – mitochondrial encephalomyopathy with
lactic acidosis – reticulated hyperpigmentation 
JAAD
41:469–473, 1999
Mendes da Costa syndrome – hereditary bullous dystrophy,
macular type; similar skin changes as Kindler’s syndrome
(Da Costa’s) syndrome 
Ped Derm 6:91–101, 1989
Mitochondrial disease – reticulated hyperpigmentation
Pediatrics 103:428–433, 1999
Naegeli–Franceschetti–Jadassohn syndrome – autosomal
dominant, reticulate gray to brown pigmentation of neck, upper
trunk and flexures, punctate or diffuse palmoplantar
keratoderma, hypohidrosis with heat intolerance, onycholysis,
subungual hyperkeratosis, yellow tooth enamel 
JAAD
28:942–950, 1993
Naegeli–Franceschetti–Jadassohn syndrome variant –
reticulate pigmentary dermatosis with hypohidrosis and short
stature 
Int J Dermatol 34:30–31, 1995
Nicolau syndrome – embolia cutis medicamentosa;
sulfonamides, benzathine penicillin, gentamicin, phenobarbital,
camphor-quinine, triflupromazine, chlorpromazine, interferon-
α
Ped Derm 12:187–190, 1995
Pachyonychia congenita
Reticulate acropigmentation of Dohi – dyschromatosis
symmetrica hereditaria 
Clin Exp Derm 20:477, 1995; autosomal
recessive 
JAAD 43:113–117, 2000
Reticulate acropigmentation of Kitamura 
Dermatology
200:57–58, 2000; Dermatology 195:337–343, 1997;
JAAD 37:884–886, 1997; Int J Dermatol 32:726–727, 1993;
BJD 109:105–110, 1983; BJD 95:437–443, 1976
Reticular erythematous mucinosis (REM syndrome) 
BJD
150:173–174, 2004; AD 140:660–662, 2004; JAAD 19:859–868,
1988; BJD 91:191–199, 1974; AD 82:980–985, 1960
Reticulate hyperpigmentation of Iijima, Naito, and Uyeno 
Acta
DV 71:248–250, 1991
Rombo syndrome – vermiculate atrophoderma
Rothmund–Thomson syndrome
Trisomy 21 – congenital livedo reticularis 
Rook p.584, 1998,
Sixth Edition
Tumor necrosis factor (TNF) receptor 1-associated periodic
fever syndromes (TRAPS) (same as familial Hibernian fever and
familial periodic fever) – tender red plaques, fever, polycyclic,
reticulated, and migratory patches and plaques, conjunctivitis,
periorbital edema, myalgia, abdominal pain, headache; Irish and
Scottish predominance 
Pre-AAD Pediatric Dermatology
Meeting, March 2000
Weary’s syndrome – hereditary and bullous acrokeratotic
poikiloderma of Weary and Kindler
Woolly hair, alopecia, premature loss of teeth, nail dystrophy,
reticulate acral hyperkeratosis, facial abnormalities 
BJD
145:157–161, 2001
Ziprkowski–Margolis syndrome