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A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1



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[Encyclopedia of Differential Diagnosis in Dermatology] Paul Schneiderman, Marc E. Grossman - A Clinician\'s Guide to Dermatologic Differential Diagnosis, Volume 1 The Text (Encyclopedia of Differential Diagnosis in D

278
A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Schneiderman page 200-300.qxd 5/16/2006 6:49 PM Page 278


plugged pit; may be verrucous; filiform; anhidrotic or
hyperhidrotic; most common on palms and soles 
JAAD
43:364–367, 2000; JAAD 24:300–1, 1991; Cutis 46:495–497,
1990
Radiation
Rapp–Hodgkin ectodermal dysplasia – autosomal dominant;
sparse hair, nails narrow and dystrophic, small stature, cleft lip
or palate, hypospadias, conical teeth and hypodontia; distinctive
facies 
Ped Derm 7:126–131, 1990; J Med Genet 15:269–272,
1968
Ross syndrome 
Ghatan p.238, 2002, Second Edition
Rosselli–Gulinetti syndrome – autosomal recessive,
hypohidrosis, fine, dry, sparse scalp hair, dystrophic nails and
teeth, cleft lip and palate, syndactyly, defects of external
genitalia 
J Plast Surg 14:190–204, 1961
Rothmund–Thomson syndrome 
Dermatology 196:260–263, 1998
Sandmann–Andra syndrome – autosomal dominant,
hypohidrosis, hypodontia 
Z Kinderheilk 82:238–255, 1959
Scleroderma 
Rook p.1997, 1998, Sixth Edition
Simple anhidrosis 
Am J Dis Child 113:477–479, 1967
Sjögren’s syndrome – secondary acquired generalized
anhidrosis 
BJD 150:589–593, 2004; Clin Rheumatol
19:396–397, 2000; JAAD 16:233–235, 1987; with
syringolymphoid hyperplasia 
JAAD 35:350–352, 1996
Sunstroke
Sweat gland fatigue 
Rook p.1997, 1998, Sixth Edition
Systemic disorders
Toxic
Typhoid fever – post-typhoid anhidrosis 
Postgrad Med J
71:435–436, 1995
Xeroderma–talipes–enamel defect (Moynahan syndrome) –
hypohidrosis, nail dystrophy, cleft palate, bilateral talipes,
mental deficiency 
Proc R Soc Med 63:447–448, 1970
X-linked reticulate pigmentary disorder with systemic
manifestations (familial cutaneous amyloidosis) (Partington
syndrome II) – X-linked; rare; Xp21–22; boys with generalized
reticulated muddy brown pigmentation (dyschromatosis) with
hypopigmented corneal dystrophy (dyskeratosis), coarse unruly
hair, unswept eyebrows, silvery hair, hypohidrosis, recurrent
pneumonia with chronic obstructive disease, clubbing; failure to
thrive, female carriers with linear macular nevoid Blascko-esque
hyperpigmentation 
Ped Derm 22:122–126, 2005; Semin Cut
Med Surg 16:72–80, 1997; Am J Med Gen 10:65, 1981

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