PALLER AND MANCINI HURWITZ CLINICAL PEDIATRIC DERMATOLOGY 6TH EDITION PDF FREE DOWNLOAD:

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This book written by two leaders in the field of pediatric dermatology, this classic text provides both detailed content for the specialist and easily accessible information for the non-dermatologist and less experienced clinician. Paller and Mancini – Hurwitz Clinical Pediatric Dermatology, 6th Edition, comprehensively covers the full range of skin disorders in children, offering authoritative, practical guidance on diagnosis and treatment in a single volume. This award-winning, evidence-based text has been fully revised and updated, and is an essential resource for anyone who sees children with skin disorders.

Features of Paller and Mancini – Hurwitz Clinical Pediatric Dermatology 6th Edition PDF:

Following are the features of this book given below;

• Features new content outline boxes for faster navigation, hundreds more clinical images, and authors’ tips for the diagnosis and treatment of pediatric skin diseases.
• Contains updated, evidence-based guidance and the latest drug developments and disease classifications.
• Provides a careful balance of narrative text, useful tables, and 1,300 high-quality clinical photographs, helping you recognize virtually any skin condition you’re likely to see.
• Includes a greatly expanded discussion of atopic dermatitis and psoriasis and new therapeutic approaches for treating genetic disorders and systemic diseases such as ichthyoses and rheumatologic disorders.
• Discusses new tests for subclassifying disease, such as the myositis-specific antibodies of juvenile dermatomyositis, genotyping, and immunophenotypes of inflammatory skin disorders.
• Contains new and updated tables on psoriasis co-morbidities, genetic syndrome classifications, acne therapies, pediatric histiocytoses, PHACE syndrome criteria, HSV therapies and juvenile dermatomyositis.
• Features updated sections on infections, exanthems, vascular disorders, dermatoses and genodermatoses.
• Discusses hot topics such as the use of stem cell and cell therapy, as well as recombinant protein, for treating epidermolysis bullosa; the resurgence of measles; congenital Zika virus infections; and much more.

Table of Contents:

• 1.  An overview of dermatologic diagnosis and procedures
•     Configuration of lesions
•     Distribution and morphologic patterns of common skin disorders
•     Changes in skin color
•     Racial variations in the skin and hair
•     Procedures to aid in diagnosis
•     Therapeutic procedures
•     Key references
•     References
• 2.  Cutaneous disorders of the newborn
•     Neonatal skin
•     Physiologic phenomena of the newborn
•     Cephalohematoma
•     Caput succedaneum
•     Complications from fetal and neonatal diagnostic procedures
•     Abnormalities of subcutaneous tissue
•     Miscellaneous cutaneous disorders
•     Developmental abnormalities of the newborn
•     Congenital infections of the newborn
•     Key references
•     References
• 3.  Eczematous eruptions in childhood
•     Atopic dermatitis
•     Pityriasis alba
•     Hyperimmunoglobulinemia E syndrome
•     Wiskott–Aldrich syndrome
•     Lichen simplex chronicus
•     Seborrheic dermatitis
•     Intertrigo
•     Dyshidrotic eczema
•     Juvenile plantar dermatosis
•     Frictional lichenoid dermatitis
•     Nummular dermatitis
•     Winter eczema
•     Lichen striatus
•     Contact dermatitis
•     Key references
•     References
• 4.  Papulosquamous and related disorders
•     Childhood psoriasis
•     Reactive arthritis
•     Pityriasis rubra pilaris
•     Pityriasis lichenoides
•     Pityriasis rosea
•     Lichen planus
•     Lichen nitidus
•     Keratosis lichenoides chronica
•     Key references
•     References
• 5.  Hereditary disorders of cornification (the ichthyoses and palmoplantar keratodermas)
•     Nonsyndromic forms of ichthyosis
•     Syndromic forms of ichthyosis
•     Treatment of nonsyndromic and syndromic ichthyoses
•     Other disorders of differentiation
•     Porokeratoses
•     Palmoplantar keratodermas
•     Key references
•     References
• 6.  Hereditary disorders of the dermis
•     Ehlers–Danlos syndrome
•     Marfan syndrome
•     Osteogenesis imperfecta
•     Cutis laxa
•     Pseudoxanthoma elasticum
•     Elastosis perforans serpiginosa
•     Focal dermal hypoplasia
•     Laminopathies
•     Restrictive dermopathy
•     Werner syndrome
•     Stiff skin syndrome
•     Winchester syndrome
•     Buschke–Ollendorff syndrome
•     Lipoid proteinosis
•     Infantile systemic hyalinosis and juvenile hyaline fibromatosis
•     Key references
•     References
• 7.  Disorders of hair and nails
•     Hair
•     Neonatal hair
•     Tools for diagnosis of hair loss disorders
•     Alopecias
•     Eruptive vellus hair cysts
•     Hypertrichosis and hirsutism
•     Pigmentary changes of hair
•     Nails
•     Key references
•     References
• 8.  Acne vulgaris and other disorders of the sebaceous and sweat glands
•     Disorders of the sebaceous glands
•     Disorders of the apocrine glands
•     Disorders of the eccrine glands
•     Key references
•     References
• 9.  Cutaneous tumors and tumor syndromes
•     Pigmented lesions
•     Melanocytic nevi
•     Tumors of the epidermis
•     Tumors of the oral mucosa
•     Tumors of the epidermal appendages
•     Dermal tumors
•     Fibromatoses
•     Tumors of fat, muscles, and bone
•     Miscellaneous
•     Key references
•     References
• 10.  Histiocytoses and malignant skin diseases
•     Langerhans cell histiocytosis
•     Juvenile Xanthogranuloma
•     Xanthoma Disseminatum
•     Benign Cephalic Histiocytosis
•     Necrobiotic Xanthogranuloma
•     Generalized Eruptive Histiocytoma
•     Progressive nodular histiocytoma
•     Multicentric reticulohistiocytosis
•     Hemophagocytic lymphohistiocytosis
•     Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease)
•     Cutaneous pseudolymphoma
•     Leukemia cutis
•     Lymphomatoid papulosis
•     Lymphoma cutis
•     Cutaneous T-cell lymphoma
•     Neuroblastoma
•     Rhabdomyosarcoma
•     Key references
•     References
• 11.  Disorders of pigmentation
•     Disorders of abnormal pigmentation
•     Disorders of hyperpigmentation
•     Key references
•     References
• 12.  Infantile hemangiomas, vascular malformations, and other vascular disorders of infancy and childhood
•     Classification of vascular lesions
•     Vascular tumors and tumor syndromes
•     Vascular malformations and malformation syndromes
•     Disorders of lymphatic vessels
•     Disorders associated with vascular dilation or constriction
•     Pigmented purpuric eruptions
•     Purpura fulminans
•     Gardner–Diamond syndrome
•     Scurvy
•     Key references
•     References
• 13.  Bullous disorders of childhood
•     Hereditary blistering disorders
•     Key references
•     References
• 14.  Bacterial, mycobacterial, and protozoal infections of the skin
•     Bacterial infections
•     Nontuberculous (“atypical”) mycobacterial infections
•     Tuberculosis of the skin
•     The tuberculid disorders
•     Leprosy
•     Anthrax
•     Cat-scratch disease
•     Disorders resulting from fungus-like bacteria
•     Treponemal infections
•     Protozoal disorders
•     Key references
•     References
• 15.  Viral diseases of the skin
•     Herpes simplex virus infection
•     Herpes zoster
•     Viral-like disorders of the oral mucosa
•     Warts
•     Molluscum contagiosum
•     Cowpox and pseudocowpox
•     Orf
•     Smallpox
•     Acquired immunodeficiency syndrome in children
•     Key references
•     References
• 16.  Exanthematous diseases of childhood
•     Varicella (chickenpox)
•     Rubeola (measles)
•     Scarlet fever
•     Rubella (German measles)
•     Filatow–Dukes disease
•     Erythema infectiosum
•     Roseola infantum
•     Other viral exanthems
•     Exanthems associated with mycoplasma pneumoniae infection
•     Rickettsial diseases
•     Key references
•     References
• 17.  Skin disorders caused by fungi
•     Superficial fungal infections
•     Candidiasis
•     Deep fungal disorders
•     Key references
•     References
• 18.  Infestations, bites, and stings
•     Arthropods
•     Other cutaneous parasites
•     Seabather’s eruption
•     Jellyfish stings
•     Key references
•     References
• 19.  Photosensitivity and photoreactions
•     Tanning and sunburn reactions
•     Photodermatoses
•     Photosensitivity induced by exogenous sources
•     Genetic disorders associated with photosensitivity
•     Pellagra
•     The porphyrias
•     Key references
•     References
• 20.  Urticarias and other hypersensitivity disorders
•     Allergic reactions
•     Urticaria
•     Contact urticaria
•     Physical urticarias
•     Anaphylaxis
•     Angioedema
•     C1 inhibitor–hereditary angioneurotic edema
•     Scombroid and ciguatera fish poisoning
•     Serum sickness and serum sickness–like reactions
•     Exanthematous eruptions
•     Drug reaction with eosinophilia and systemic symptoms
•     Stevens–Johnson syndrome and toxic epidermal necrolysis
•     Reactive infectious mucocutaneous or mucosal-predominant eruption
•     Fixed drug eruption
•     Acute generalized exanthematous pustulosis
•     Erythema multiforme
•     Annular erythemas
•     Panniculitis
•     Erythema nodosum
•     Eccrine hidradenitis
•     Cutaneous reactions to cold
•     Cutaneous reactions to heat
•     Sweet syndrome (acute febrile neutrophilic dermatosis)
•     Bowel-associated dermatosis-arthritis syndrome
•     Hypereosinophilic syndrome
•     Wells syndrome
•     Pregnancy and pregnancy-related dermatoses
•     Autoimmune progesterone dermatitis
•     Key references
•     References
• 21.  Vasculitic disorders
•     Henoch–Schönlein (anaphylactoid) purpura
•     Acute hemorrhagic edema of infancy
•     Hypersensitivity vasculitis
•     Urticarial vasculitis
•     Cryoglobulinemic vasculitis
•     Necrotizing vasculitis with granulomas
•     Erythema elevatum diutinum
•     Polyarteritis nodosa
•     Kawasaki disease
•     Key references
•     References
• 22.  Collagen vascular disorders
•     Juvenile idiopathic arthritis
•     Systemic lupus erythematosus
•     Cutaneous lupus erythematosus
•     Nonspecific clinical manifestations of SLE
•     Laboratory features in the diagnosis of SLE
•     Drug-induced lupus erythematosus
•     Prognosis and therapy for SLE
•     Neonatal lupus erythematosus
•     Antiphospholipid antibody syndrome
•     Degos disease
•     Juvenile dermatomyositis
•     Systemic sclerosis (scleroderma)
•     Eosinophilic fasciitis
•     Nephrogenic systemic fibrosis
•     Scleredema
•     Morphea
•     Lichen sclerosus et atrophicus
•     Anetoderma
•     Relapsing polychondritis
•     Sjögren syndrome
•     Mixed connective tissue disease
•     Key references
•     References
• 23.  Endocrine disorders and the skin
•     Thyroid disorders
•     Parathyroid disorders
•     Disorders of the adrenal glands
•     Disorders of androgen excess
•     Gonadal dysgenesis/Turner syndrome
•     Pituitary disorders
•     Multiple Endocrine Neoplasia Syndromes
•     Autoimmune Polyglandular syndromes
•     Mccune–Albright syndrome
•     Disorders associated with diabetes mellitus
•     Scleredema diabeticorum
•     Glucagonoma syndrome
•     Key references
•     References
• 24.  Inborn errors of metabolism
•     Phenylketonuria
•     Disorders of tyrosine metabolism
•     Cobalamin deficiency
•     Homocystinuria
•     Trimethylaminuria
•     Wilson disease (Hepatolenticular degeneration)
•     Lesch–Nyhan syndrome
•     Dermatitis from nutritional abnormalities
•     Disorders that resemble acrodermatitis enteropathica
•     The hyperlipidemias
•     The mucopolysaccharidoses
•     Other storage disorders
•     Key references
•     References
• 25.  Skin signs of other systemic diseases
•     Primary immunodeficiency disorders
•     Graft-Versus-Host Disease
•     Anorexia nervosa and bulimia
•     Autoinflammatory disorders
•     Polygenic forms of autoinflammatory disorders
•     Amicrobial pustulosis of the folds
•     Behçet disease
•     Sarcoidosis
•     Other inflammasomopathies
•     Inflammasomopathies with pyoderma gangrenosum
•     CANDLE syndrome
•     The ubiquitinopathies (relopathies)
•     LUBAC component deficiency
•     Key references
•     References
• 26.  Abuse and factitial disorders
•     Child abuse
•     Factitial skin disorders
•     Cutaneous mimickers of abuse and factitial disorders
•     Key references
•     References
• Index

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