Schneiderman Prelims Vol-I. qxd

INFILTRATIVE DISORDERS
Langerhans cell histiocytosis
Mastocytosis
INFLAMMATORY DISEASES
Eosinophilic gastroenteritis
Toxic epidermal necrolysis
METABOLIC DISEASES
Acrodermatitis enteropathica
Aminoaciduria – methylmalonic, arginino – succinicaciduria,
maple syrup urine disease (MSUD), propionic acidemia
Argininosuccinicaciduria
Biotinidase deficiency 
AD 136:875–880, 2000
Carbamoyl phosphate synthetase deficiency
Carbohydrate deficient glycoprotein syndromes
Citrullinemia 
AD 136:875–880, 2000
Cobalamin deficiency
Cystic fibrosis
Essential fatty acid deficiency
Gaucher’s disease – collodion babies 
Arch Dis Child 66:667,
1991
Holocarboxylase deficiency
Maple syrup urine disease 
AD 129:384–385, 1993
Methylmalonicacidemia – perioral erosions
Porphyria – transient erythropoietic protoporphyria
JAAD
35:833–834, 1996
Propionic acidemia
Protein malnutrition
Secretory IgA deficiency 
AD 136:875–880, 2000
Zinc deficiency
NEOPLASTIC DISEASES
Leukemia – acute lymphocytic leukemia
PHOTOSENSITIVITY DISORDERS
Chronic actinic dermatitis 
Bolognia p.166, 2004
PRIMARY CUTANEOUS DISEASES
Atopic dermatitis 
Bolognia p.171, 2004
Bullous congenital ichthyosiform erythroderma (epidermolytic
hyperkeratosis) 
JID 91:357–361, 1993
Erythrokeratoderma variabilis 
Ped Derm 12:351–354, 1995
Harlequin infant – presenting as non-bullous congenital
ichthyosiform erythroderma 
BJD 135:448–453, 1996
Ichthyosis
Lamellar ichthyosis 
AD 136:875–880, 2000
Non-bullous congenital ichthyosiform erythroderma 
AD
136:875–880, 2000
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A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
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Psoriasis 
AD 136:875–880, 2000; Ped Derm 12:231–234, 1995
Seborrheic dermatitis 
AD 136:875–880, 2000