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Atlas of Genodermatoses [Kõva köide]

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  • Formaat: Hardback, 424 pages, kõrgus x laius: 285x214 mm, kaal: 1928 g, 910 Illustrations, color
  • Ilmumisaeg: 12-Dec-2005
  • Kirjastus: CRC Press
  • ISBN-10: 1841842516
  • ISBN-13: 9781841842516
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Atlas of GenodermatosesSuurem pilt
  • Formaat: Hardback, 424 pages, kõrgus x laius: 285x214 mm, kaal: 1928 g, 910 Illustrations, color
  • Ilmumisaeg: 12-Dec-2005
  • Kirjastus: CRC Press
  • ISBN-10: 1841842516
  • ISBN-13: 9781841842516
Teised raamatud teemal:
Püsilink: https://www.kriso.ee/db/9781841842516.html
Märksõnad:
A lavishly illustrated guide to almost 200 inherited diseases of the skin, hair, and nails. Each entry includes synonyms, age of onset, clinical findings, complications, course, laboratory findings, diagnosis, therapy, and key references, adding up to far more than just a collection of photographs. In addition to being a clinical primer, this is also a work of scientific research and contains the first printed description of two new syndromes. The fast-moving world of genetic research means that the latest genetic correlations, included here, render previous texts out of date. All specialists in Dermatology and Pediatrics should find this an invaluable front-line resource in the clinic.
Preface xi
Foreword xiii
Rudolf Happle
Illustration credits
xv
Epidermolysis bullosa
Epidermolytic epidermolysis bullosa (EEB)
1(4)
Junctional epidermolysis bullosa (JEB)
5(4)
Dermolytic epidermolysis bullosa
9(6)
Epidermolytic hyperkeratoses
`Classical' epidermolytic hyperkeratosis
15(4)
Ichthyosis bullosa of Siemens
19(1)
Ichthyosis Curth--Macklin
20(2)
`Stellate' epidermolytic hyperkeratosis
22(3)
Acantholytic diseases
Darier's disease
25(4)
Acrokeratosis verruciformis
29(1)
Hailey--Hailey disease
30(2)
Peeling skin syndrome
32(3)
Ichthyoses
Dominant ichthyosis
35(3)
X-linked ichthyosis
38(2)
Self-healing collodion baby
40(2)
Lamellar ichthyosis
42(6)
Harlequin fetus
48(2)
Pityriasis rotunda
50(1)
Congenital reticular ichthyosiform erythroderma (CRIE)
51(2)
Syndromic ichthyoses
Netherton syndrome
53(4)
Sjogren--Larsson syndrome
57(1)
Refsum syndrome
58(1)
Trichothiodystrophy
59(4)
Dorfman--Chanarin syndrome
63(2)
Erythrokeratodermas
Erythrokeratoderma variabilis
65(2)
Symmetric progressive erythrokeratoderma
67(2)
Palmoplantar keratodermas
Epidermolytic palmoplantar keratoderma
69(1)
Unna--Thost palmoplantar keratoderma
70(2)
Keratoderma hereditaria mutilans
72(2)
Greither's disease
74(1)
Olmsted's syndrome
75(2)
Papillon--Lefevre syndrome
77(2)
Huriez's syndrome
79(1)
Mal de Meleda
80(2)
Punctate palmoplantar keratoderma
82(2)
Striate keratoderma
84(1)
Richner--Hanhart syndrome
85(2)
Painful callosities
87(1)
Pachydermoperiostosis
88(1)
Akrokeratoelastoidosis
89(1)
Naxos syndrome
90(3)
Other disorders of keratinization
Porokeratoses
93(4)
Kyrle's disease
97(1)
Child syndrome
98(2)
X-linked dominant chondrodysplasia punctata
100(2)
KID syndrome
102(2)
Pityriasis rubra pilaris
104(3)
Poikilodermas and aging syndromes
Kindler's syndrome
107(3)
Xeroderma pigmentosum
110(3)
Rothmund--Thomson syndrome
113(1)
Naegeli--Franceschetti syndrome
114(2)
Werner's syndrome
116(1)
Hutchinson--Gilford syndrome
117(2)
Kitamura--Dowling--Degos disease
119(2)
Cockayne's syndrome
121(2)
Hair diseases
Alopecias
Marie--Unna hypotrichosis
123(1)
Hypotrichosis simplex of the scalp
124(1)
Ichthyosis follicularis with atrichia and photophobia
125(2)
Alopecia areata
127(1)
Ulerythema ophryogenes
128(2)
Triangular alopecia
130(1)
Hirsutism
Hypertrichosis congenita
131(2)
Localized hypertrichosis
133(1)
Hair shaft abnormalities
Monilethrix
134(2)
Pili annulati
136(1)
Pili torti
137(2)
Woolly hair
139(1)
Elejalde's syndrome
140(1)
Griscelli's syndrome
141(2)
Uncombable hair syndrome
143(1)
Menkes' kinky hair syndrome
144(1)
Trichorhinophalangeal syndrome
145(1)
Atrichia with papular lesions
146(2)
Loose anagen syndrome
148(1)
Keratosis follicularis spinulosa decalvans
149(2)
Nail disorders
Pachyonychia congenita
151(3)
Nail--patella--elbow syndrome
154(2)
Twenty-nail dystrophy
156(1)
Malalignment of the great toenails
157(1)
Leukonychia
158(1)
Pterygium inversum of nails
159(1)
Iso--Kikuchi syndrome
160(1)
Sebocystomatosis
161(108)
Oral mucosa
White sponge nevus
165(1)
Dyskeratosis congenita
166(3)
Oral-facial-digital syndrome type I
169(2)
Neurocutaneous syndromes
Neurofibromatosis type 1
171(7)
Neurofibromatosis type 2
178(1)
Noonan's syndrome
179(1)
Tuberous sclerosis complex
180(7)
Cardiofacio-cutaneous syndrome
187(1)
Phakomatosis pigmentokeratotica
188(4)
Epidermal nevi and epidermal nevus syndromes
192(4)
Waxy keratosis of childhood
196(2)
Papular epithelial hamartomas and neurologic abnormalities syndrome
198(2)
Proteus syndrome
200(3)
Ectodermal dysplasias and related disorders
Ectodermal dysplasias
203(24)
Hypohidrotic ectodermal dysplasia
203(5)
Rapp--Hodgkin--AEC, EEC syndrome, limb--mammary disease, adult-spectrum ectodermal dysplasia
208(4)
Tricho-dento-osseous syndrome
212(1)
Witkop's syndrome
213(1)
Ellis--Van Creveld--Weyers acrodental dysostosis complex
214(2)
Cleft lip--palate with ectodermal dysplasia syndrome
216(1)
Clouston's disease
217(2)
Ectodermal dysplasia--skin fragility syndrome
219(1)
Pure hair--nail ectodermal dysplasia
220(2)
Incontinentia pigmenti
222(5)
`Ectomesodermal' dysplasias
Goltz's syndrome
227(4)
MIDAS syndrome
231(2)
Fatty tissue anomalies
Launois--Bensaude syndrome
233(1)
Total lipodystrophy
234(2)
Partial lipodystrophy
236(3)
Disorders of connective tissue
Ehlers--Danlos syndromes
239(8)
Cutis laxa
247(2)
Pseudoxanthoma elasticum
249(2)
Marfan's syndrome
251(2)
Connective tissue nevi and Buschke--Ollendorff syndrome
253(2)
Elastosis perforans serpiginosa
255(1)
Costello's syndrome
256(1)
Michelin tire baby
257(1)
Juvenile hyaline fibromatosis
258(2)
Cutaneous mastocytosis
260(1)
Cutaneous leiomyomatosis
261(1)
Restrictive dermopathy
262(1)
Dermochondrocorneal dystrophy
263(1)
Progressive osseous heteroplasia
264(2)
Cutis verticis gyrata
266(3)
Aplasia cutis
269(124)
Disorders of pigmentation
Oculocutaneous albinisms
275(4)
Hermansky--Pudlak syndrome
279(1)
Hypomelanosis of Ito
280(1)
Piebaldism
281(2)
Waardenburg's syndrome
283(1)
McCune--Albright syndrome
284(2)
Linear and figurated hypo- and hyperpigmented nevi
286(3)
Segmental lentiginosis
289(3)
Leopard syndrome
292(2)
Ota nevus
294(1)
Cutis tricolor
295(1)
Dyschromatosis symmetrica hereditaria
296(1)
Vascular disorders
Complex of Sturge--Parkes--Weber, Klippel--Trenaunay and Cobb's syndromes
297(1)
Sturge--Weber syndrome
297(3)
Klippel--Trenaunay syndrome
300(2)
Cobb's syndrome
302(1)
Von Hippel--Lindau syndrome
303(1)
Ataxia telangiectasia
304(2)
Hemorrhagic telangiectasia
306(2)
Cutis marmorata telangiectatica congenita
308(3)
Maffucci syndrome
311(1)
Blue rubber bleb nevus syndrome
312(2)
Diffuse benign telangiectasia and port-wine stains complex
314(1)
Unilateral nevoid and generalized `essential' telangiectasia
315(3)
Nevus anemicus
318(1)
Phakomatosis pigmentovascularis
319(2)
Lymphedema
321(1)
Generalized cyanosis, phlebectases and soft skin syndrome
322(2)
Glomuvenous malformation
324(3)
Metabolic disease
Porphyria cutanea tarda and hepatoerythropoietic porphyria
327(3)
Erythropoietic protoporphyria
330(2)
Erythropoietic porphyria
332(2)
Acrodermatitis enteropathica
334(1)
Fabry's disease
335(2)
Sea-blue histiocytosis
337(2)
Cerebrotendinous xanthomatosis
339(2)
Prolidase deficiency
341(1)
Methylmalonic aciduria
342(3)
Immunodeficiency disorders
Omenn's syndrome
345(2)
Hyper IgE syndrome
347(1)
C1q esterase inhibitor deficiency
348(1)
Chediak--Higashi syndrome
349(2)
Complex malformative syndromes with distinctive cutaneous signs
Rubinstein--Taybi syndrome
351(2)
Cornelia de Lange syndrome
353(2)
Cohen's syndrome
355(1)
Branchio-oculofacial syndrome
356(2)
Barber--Say syndrome
358(1)
Turner's syndrome
359(2)
Pallister--Killian syndrome
361(2)
Encephalocraniocutaneous lipomatosis
363(1)
GAPO syndrome
364(3)
Genodermatoses related to malignancy
Nevoid basal cell carcinoma syndrome
367(2)
Muir--Torre syndrome
369(2)
Cowden's syndrome
371(2)
Gardner syndrome
373(1)
Bloom's syndrome
374(2)
Howel--Evans syndrome
376(1)
Multiple endocrine neoplasia syndrome, type 2b
377(1)
Peutz--Jeghers syndrome
378(2)
Birt--Hogg--Dube syndrome
380(2)
Carney's complex
382(1)
Bazex--Dupre--Christol syndrome
383(2)
Epidermodysplasia verruciformis
385(1)
Brooke--Spiegler syndrome
386(2)
Progressive mucinous histiocytosis
388(1)
Degos' disease
389(2)
Rombo syndrome
391(2)
Cutaneous mosaicism
393(14)
Index 407


Ruggero Caputo and Gianluca Tadini are both from the Institute of Dermatological Science, University of Milan, Italy.